What Clinical Microbiologist Jobs are in Kenya?
Showing 9 Clinical Microbiologist jobs in Kenya
Senior Clinical Pharmacologist (Remote)
30400 Bungoma / Remote
Placements24
Posted 16 days ago
Job Viewed
Job Description
About the Role Our client, a world-renowned leader in pharmaceutical innovation, is actively searching for a highly qualified Senior Clinical Pharmacologist to join their cutting-edge research and development team. This position is entirely remote, allowing you to contribute your specialized knowledge from anywhere in Kenya. As a Senior Clinical Pharmacologist, you will be at the forefront of designing and executing clinical pharmacology studies, focusing on understanding drug metabolism, pharmacokinetics (PK), and pharmacodynamics (PD) in various patient populations. Your contributions will be vital in optimizing drug dosage, efficacy, and safety profiles, ultimately shaping the development of new therapies within the **pharmaceutical industry**. This role requires advanced scientific expertise and a dedication to rigorous research in a **remote-first environment**. Key Responsibilities
- Design, develop, and execute clinical pharmacology study protocols, including first-in-human (FIH) studies, dose-escalation studies, and drug-drug interaction studies.
- Analyze and interpret pharmacokinetic (PK) and pharmacodynamic (PD) data to characterize the drug's behavior in the body and its effects.
- Develop and validate bioanalytical methods for quantifying drug and metabolite concentrations in biological matrices.
- Contribute to regulatory submissions by preparing clinical pharmacology sections of Investigational New Drug (IND) applications, New Drug Applications (NDAs), and other relevant documents.
- Collaborate with cross-functional teams, including clinical development, biostatistics, preclinical research, and regulatory affairs, to integrate pharmacology data into overall development strategies.
- Stay abreast of the latest advancements in clinical pharmacology, drug metabolism, and relevant therapeutic areas.
- Mentor junior scientists and provide scientific leadership within the clinical pharmacology group.
- Contribute to the selection of appropriate doses and dosing regimens for further clinical development.
- Ensure all study conduct adheres to Good Clinical Practice (GCP) and relevant regulatory guidelines.
- PhD or PharmD degree in Pharmacology, Clinical Pharmacology, Pharmaceutical Sciences, or a related field.
- Minimum of 6 years of hands-on experience in clinical pharmacology within the **pharmaceutical industry** or a relevant academic setting.
- Proven expertise in designing, executing, and analyzing PK/PD studies.
- Strong understanding of drug metabolism, transporter kinetics, and bioanalytical methodologies.
- Experience with regulatory requirements for clinical pharmacology data (e.g., FDA, EMA guidelines).
- Excellent scientific writing and communication skills, with the ability to present complex data clearly.
- Proficiency in relevant software (e.g., Phoenix WinNonlin, R) for PK/PD analysis.
- Ability to work independently, manage multiple research projects, and collaborate effectively in a remote setting.
- Highly attractive salary and performance-based bonus structure.
- Comprehensive medical, dental, and vision insurance plans.
- Generous paid time off and holidays.
- Opportunities for international collaboration and professional development.
- Access to state-of-the-art research tools and technologies.
- Fully remote work arrangement with support for home office needs.
- Dynamic and intellectually stimulating work environment.
- Opportunity to contribute to the development of life-changing medicines.
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0
Job Description
About the Role Our client, a leading pharmaceutical research company, is seeking an experienced Biostatistician to join their dedicated clinical trials team in Mlolongo, Machakos, Kenya . This role is essential for the statistical design, analysis, and reporting of clinical studies. You will work closely with clinical scientists, data managers, and other statisticians to ensure the integrity and validity of research findings. The ideal candidate will possess a strong understanding of statistical methodologies relevant to clinical trials, proficiency in statistical software, and the ability to translate complex statistical concepts into clear, actionable insights. This position offers a fantastic opportunity to contribute to life-saving medical research within a dynamic and collaborative environment located in Mlolongo . We are looking for a highly analytical and detail-oriented individual who is passionate about leveraging data to advance medical knowledge and improve patient outcomes. This role requires your presence in our Mlolongo office to foster close collaboration with the on-site clinical research teams. Key Responsibilities
- Design statistical analysis plans (SAPs) for clinical trials, including defining endpoints, sample size calculations, and statistical methods.
- Perform statistical analyses of clinical trial data using SAS, R, or other statistical software.
- Interpret statistical results and prepare tables, figures, and listings for study reports and publications.
- Collaborate with clinical operations and data management teams to ensure data quality and integrity.
- Contribute to the development of study protocols and case report forms (CRFs).
- Provide statistical input for regulatory submissions and interactions with health authorities.
- Stay up-to-date with statistical methodologies and regulatory guidelines relevant to clinical trials.
- Review and critique statistical methods and results generated by others.
- Participate in cross-functional team meetings and contribute statistical expertise.
- Ensure adherence to statistical standards and best practices.
- Master's degree or Ph.D. in Biostatistics, Statistics, or a related quantitative field.
- Minimum of 3 years of experience in biostatistics, with a focus on clinical trial design and analysis.
- Proficiency in statistical programming languages such as SAS and R.
- Strong knowledge of statistical methods commonly used in clinical trials (e.g., survival analysis, longitudinal data analysis, mixed models).
- Experience with CDISC standards (SDTM, ADaM) is highly desirable.
- Understanding of regulatory requirements for clinical trials (e.g., FDA, EMA).
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills, with the ability to explain complex statistical concepts clearly.
- Ability to work effectively in a team environment and manage multiple projects.
- Experience with data visualization tools is a plus.
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1
Biostatistician - Clinical Trials & Statistical Analysis
90100 Malindi / Remote
Placements24
Posted 12 days ago
Job Viewed
Job Description
About the Role
Our client, a renowned pharmaceutical company committed to advancing global health, is seeking an experienced Biostatistician to contribute to their cutting-edge clinical research endeavors. This is a fully remote role where you will apply advanced statistical methodologies to the design of clinical trials and the analysis of clinical trial data. Your expertise will be essential in ensuring the integrity and validity of clinical study results, which are critical for regulatory submissions and scientific publications. This position offers a unique opportunity to work on diverse therapeutic areas and collaborate with a world-class team of researchers and clinicians from the convenience of your home office. We value scientific rigor and are looking for a dedicated professional to join our mission of bringing life-saving treatments to patients.
Key Responsibilities- Provide statistical expertise in the design and planning of clinical trials, including sample size determination, randomization schemes, and statistical analysis plans (SAPs).
- Develop and implement statistical analysis methods for clinical trial data.
- Perform statistical analyses using SAS or R, ensuring accuracy and adherence to SAPs.
- Interpret statistical results and contribute to the preparation of clinical study reports (CSRs), regulatory submission documents, and scientific publications.
- Collaborate with clinical teams, data management, and other functions to ensure data quality and integrity.
- Contribute to the development and maintenance of statistical programming standards and best practices.
- Review study protocols and other study-related documents from a statistical perspective.
- Stay current with advancements in biostatistics, statistical software, and regulatory requirements related to clinical trials.
- Present statistical findings to internal and external stakeholders, including regulatory agencies.
- Ensure all statistical activities are conducted in compliance with regulatory guidelines (e.g., ICH) and company SOPs.
- Master's or Ph.D. degree in Biostatistics, Statistics, or a closely related quantitative field.
- Minimum of 4 years of experience in biostatistics within the pharmaceutical or biotechnology industry, focusing on clinical trial analysis.
- Proficiency in statistical programming languages such as SAS (preferred) or R.
- Strong understanding of clinical trial design, statistical methodologies, and regulatory requirements (e.g., ICH E9).
- Experience with various statistical techniques, including survival analysis, regression modeling, and longitudinal data analysis.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills, with the ability to clearly explain complex statistical concepts.
- Ability to work independently, manage multiple projects, and meet strict deadlines in a remote setting.
- Familiarity with clinical data standards (e.g., CDISC) is a plus.
- Detail-oriented with a commitment to scientific rigor and accuracy.
- Competitive salary and comprehensive benefits package.
- Health, dental, and vision insurance.
- Retirement savings plan with employer match.
- Generous paid time off and holidays.
- Opportunities for professional development and continuing education.
- Flexible remote working arrangements.
- Exposure to innovative clinical research projects across various therapeutic areas.
- A collaborative and supportive team environment.
- The opportunity to make a significant contribution to patient health.
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2
Job Description
**IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models.**
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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3
Clinical Trial Coordinator - FSP - Kenya
Nairobi
ThermoFisher Scientific
Posted 4 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join Us as a Senior Clinical Trial Coordinator - Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you'll have the opportunity to provide administrative and technical support to the Project Team. As a Senior Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements.
What You'll Do:
- According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
- Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
- Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
- Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
- Provides system support (i.e. GoBalto & eTMF).
- Supports RBM activities.
- Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
- Supports scheduling and organization of client and/or internal meetings with completion of related meeting minutes.
- Reviews and tracks local regulatory documents.
- Transmits documents to client and centralized IRB/IEC.
- Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
- Maintains vendor trackers.
- Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
- Assists with study-specific translation materials and translation QC upon request.
- May attend Kick off meeting and take notes when required.
Education and Experience Requirements:
- High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
- Bachelor's degree preferred.
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
- Ability to work in a team or independently as required
- Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
- Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
- Strong customer focus
- Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
- Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
- Excellent English language and grammar skills and proficient local language skills as needed
- Good presentation skills
- Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
- Ability to successfully complete PPD clinical training program
- Self-motivated, positive attitude with effective strong interpersonal skills
Working Conditions and Environment:
- Work is performed in an office/ laboratory/clinical/ and/or home office environment with exposure to electrical office equipment.
- Occasional drives to site locations. Potential Occasional travel required
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Join Us as a Senior Clinical Trial Coordinator - Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you'll have the opportunity to provide administrative and technical support to the Project Team. As a Senior Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements.
What You'll Do:
- According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
- Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
- Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
- Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
- Provides system support (i.e. GoBalto & eTMF).
- Supports RBM activities.
- Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
- Supports scheduling and organization of client and/or internal meetings with completion of related meeting minutes.
- Reviews and tracks local regulatory documents.
- Transmits documents to client and centralized IRB/IEC.
- Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
- Maintains vendor trackers.
- Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
- Assists with study-specific translation materials and translation QC upon request.
- May attend Kick off meeting and take notes when required.
Education and Experience Requirements:
- High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
- Bachelor's degree preferred.
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
- Ability to work in a team or independently as required
- Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
- Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
- Strong customer focus
- Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
- Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
- Excellent English language and grammar skills and proficient local language skills as needed
- Good presentation skills
- Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
- Ability to successfully complete PPD clinical training program
- Self-motivated, positive attitude with effective strong interpersonal skills
Working Conditions and Environment:
- Work is performed in an office/ laboratory/clinical/ and/or home office environment with exposure to electrical office equipment.
- Occasional drives to site locations. Potential Occasional travel required
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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4
Job Description
**Junior Medical Science Liaison**
Location: Eldoret, Kenya
Employment Type: Future Opportunity (Talent Pipeline)
**About the Opportunity**
We are building a pipeline of talented professionals for anticipated Junior Medical Science Liaison (MSL) roles. While these positions are not currently open, we invite expressions of interest from individuals passionate about medical affairs and scientific engagement. Joining our pipeline means you'll be among the first to hear about new opportunities as they arise.
**Key Responsibilities**
+ Serve as a scientific resource, supporting healthcare professionals and internal teams with evidence-based information.
+ Communicate clinical and scientific data in a clear, balanced, and non-promotional manner.
+ Support medical education and respond to medical inquiries in accordance with applicable laws and company policies.
+ Collaborate with cross-functional teams to ensure alignment on scientific communication and compliance with all regulatory requirements.
**Ideal Candidate Profile**
+ Advanced degree in life sciences (PharmD, PhD, MD, or equivalent).
+ Full Driving License.
+ Strong scientific acumen and ability to interpret clinical data.
+ Fluent skills in both local language and English
+ Excellent communication and presentation skills.
+ Interest in building professional relationships with healthcare professionals.
+ Willingness to travel within the region.
+ Commitment to upholding ethical standards and compliance with all relevant regulations and company policies.
**Why Join Our Talent Pipeline?**
+ Be the first to know about upcoming opportunities.
+ Gain insights into our company culture and medical affairs team.
+ Stay connected for future career development.
**How to Apply**
If you are interested in joining our talent pipeline, please submit your CV. We will keep you informed about relevant opportunities as they become available.
**\#LI-CES**
**\#LI-VK1**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Location: Eldoret, Kenya
Employment Type: Future Opportunity (Talent Pipeline)
**About the Opportunity**
We are building a pipeline of talented professionals for anticipated Junior Medical Science Liaison (MSL) roles. While these positions are not currently open, we invite expressions of interest from individuals passionate about medical affairs and scientific engagement. Joining our pipeline means you'll be among the first to hear about new opportunities as they arise.
**Key Responsibilities**
+ Serve as a scientific resource, supporting healthcare professionals and internal teams with evidence-based information.
+ Communicate clinical and scientific data in a clear, balanced, and non-promotional manner.
+ Support medical education and respond to medical inquiries in accordance with applicable laws and company policies.
+ Collaborate with cross-functional teams to ensure alignment on scientific communication and compliance with all regulatory requirements.
**Ideal Candidate Profile**
+ Advanced degree in life sciences (PharmD, PhD, MD, or equivalent).
+ Full Driving License.
+ Strong scientific acumen and ability to interpret clinical data.
+ Fluent skills in both local language and English
+ Excellent communication and presentation skills.
+ Interest in building professional relationships with healthcare professionals.
+ Willingness to travel within the region.
+ Commitment to upholding ethical standards and compliance with all relevant regulations and company policies.
**Why Join Our Talent Pipeline?**
+ Be the first to know about upcoming opportunities.
+ Gain insights into our company culture and medical affairs team.
+ Stay connected for future career development.
**How to Apply**
If you are interested in joining our talent pipeline, please submit your CV. We will keep you informed about relevant opportunities as they become available.
**\#LI-CES**
**\#LI-VK1**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Is this job a match or a miss?
Apply Now
5
Job Description
Job Title: Group Product Manager
Business Unit: Sun Pharma East Africa Ltd
Location: Nairobi
At Sun Pharma, we commit to helping youCreate your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each others journeys.
**JOB SUMMARY:** As a Group Product Manager (GPM) within Marketing, you will usually be office based. The **Group Product Manager (GPM)** provides **strategic leadership and end-to-end ownership** of the country brand portfolio, driving the development and execution of **HCP-focused marketing strategies** that deliver sustained **revenue growth, market share expansion, and long-term profitability** .
The role **encompasses cross-functional stakeholders** , translates market intelligence into actionable strategies, and **shapes KOL engagement and development** to strengthen brand positioning and competitive advantage. The role is accountable for **rigorous KPI governance** , excellence in execution, and continuous optimization of marketing initiatives.
**RESPONSIBILITIES:**
+ Development, collaboration, implementation, & accountability for strategic and operational plans which optimize profitability, market share, and revenue growth for a brand portfolio in the short and long term.
+ Applicant to lead various assignments to help the BU meet overall BU business goals
+ Development of marketing and promotional plans for products to support the end consumers need
+ Monitor business performance and support the portfolio with the help of regular tracking
+ Market intelligence through primary research and customer connect
+ Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups
+ Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs
+ Initiating and coordinating marketing activities and projects
+ Presentation to staff and training field staff for the sameVisiting national and international congresses, hospitals, and key opinion leaders (KOLs);
+ Translating the corporate brand strategy in close collaboration with headquarters, together with logos and visuals, working with corporate product budgets (approval for expenditure on projects, local communication strategies), and providing input into corporate product strategy;
+ Discussion partner for first, second, and third-line professionals such as medical specialists, pharmacists, and other medical professionals, and for other DMU members (decision-making units) such as local and national formulary committees and insurance companies;
+ Organizing advisory councils, acting as a discussion leader or chairman, or giving product presentations.
+ Collaboration with internal & external media to ensure the proper execution of strategies
**Job Requirements**
Educational Qualification: B. Pharm / M. Pharm & MBA
Experience: 10 to 15 years previous work experience.
Skills required include:
+ Demonstrable success in marketing or sales;
+ Strategic insight;
+ Effective networking skills and planning ability;
+ Creativity and persuasiveness;
+ Analytical and conceptual strength;
+ A strong and inspiring personality;
+ Self-starting and entrepreneurial.
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth.Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Lets create a brighter future together!
**Disclaimer:** The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Business Unit: Sun Pharma East Africa Ltd
Location: Nairobi
At Sun Pharma, we commit to helping youCreate your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each others journeys.
**JOB SUMMARY:** As a Group Product Manager (GPM) within Marketing, you will usually be office based. The **Group Product Manager (GPM)** provides **strategic leadership and end-to-end ownership** of the country brand portfolio, driving the development and execution of **HCP-focused marketing strategies** that deliver sustained **revenue growth, market share expansion, and long-term profitability** .
The role **encompasses cross-functional stakeholders** , translates market intelligence into actionable strategies, and **shapes KOL engagement and development** to strengthen brand positioning and competitive advantage. The role is accountable for **rigorous KPI governance** , excellence in execution, and continuous optimization of marketing initiatives.
**RESPONSIBILITIES:**
+ Development, collaboration, implementation, & accountability for strategic and operational plans which optimize profitability, market share, and revenue growth for a brand portfolio in the short and long term.
+ Applicant to lead various assignments to help the BU meet overall BU business goals
+ Development of marketing and promotional plans for products to support the end consumers need
+ Monitor business performance and support the portfolio with the help of regular tracking
+ Market intelligence through primary research and customer connect
+ Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups
+ Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs
+ Initiating and coordinating marketing activities and projects
+ Presentation to staff and training field staff for the sameVisiting national and international congresses, hospitals, and key opinion leaders (KOLs);
+ Translating the corporate brand strategy in close collaboration with headquarters, together with logos and visuals, working with corporate product budgets (approval for expenditure on projects, local communication strategies), and providing input into corporate product strategy;
+ Discussion partner for first, second, and third-line professionals such as medical specialists, pharmacists, and other medical professionals, and for other DMU members (decision-making units) such as local and national formulary committees and insurance companies;
+ Organizing advisory councils, acting as a discussion leader or chairman, or giving product presentations.
+ Collaboration with internal & external media to ensure the proper execution of strategies
**Job Requirements**
Educational Qualification: B. Pharm / M. Pharm & MBA
Experience: 10 to 15 years previous work experience.
Skills required include:
+ Demonstrable success in marketing or sales;
+ Strategic insight;
+ Effective networking skills and planning ability;
+ Creativity and persuasiveness;
+ Analytical and conceptual strength;
+ A strong and inspiring personality;
+ Self-starting and entrepreneurial.
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth.Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Lets create a brighter future together!
**Disclaimer:** The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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6
Job Description
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
**The Position**
**JOB OBJECTIVE(s):**
To maintain and continuously improve the afliate quality system in compliance with Roche Pharmaceutical Quality System requirements, local GxP-regulations and applicable ISO-standards whilst ensuring an uninterrupted supply of quality products to patients.
**Key Responsibilities**
**●** To conduct regular management review of the QMS by presenting and tracking performance against relevant standards
● To implement quality system in line with ISO/relevant standards by reviewing and understanding divisional SOP, analyse their impact in the local environment and effecting relevant aspects as required
● To identify discrepancies and investigate them via the available quality systems in a timely manner
● To identify and manage changes to processes, persons or systems, evaluate its impact and affected parties, implement planned actions and communicate as required
● To implement local CAPA management by identifying the probable root cause, proposing relevant corrective and/or preventative actions, executing the identied action and evaluating the effectiveness as required
● To conduct quality risk assessments using the quality risk assessment tools , identify risk areas, implementing risk mitigation/elimination measures,and monitor changes as required
● To ensure data integrity by creating, maintaining or implementing relevant SOPs
● To initiate or support quality audits by performing self-inspections, external audits. Identify audit queries, draft audit reports, engage with the relevant parties to implement corrective action and follow up on agreed actions
● To initiate annual mock recall and support actual recall process by informing the Health authority, liaising with the distributor(s) to facilitate product recall, contacting customers and reconciling the returned goods as required
● To maintain up to date knowledge of PQS by participating in physical trainings or provided in virtual learning platforms as required
● To perform training of personnel involved in GxP activities
● To maintain systems for reporting product complaints, including monitoring of the generic product complaints mailbox on business days
● To manage all complaints received based on the the applicable SOP
● Release commercial batches to the local market, and where applicable, Investigation Medicinal Products to the local clinical trial sites, according to the local regulations, Marketing Authorizations and Clinical Trial Authorizations
● To ensure all required KPI's in the product release process are met and feedback is provided as required
● To support the returns process by implementing the relevant SOP, ● Ensure compliance with GDP guidelines and local regulations for the products distributed to the market
● Support batch traceability for all batches received and distributed by the local warehouse
● Coordinate with the supply chain responsible to manage additional controls for cold chain management
● To support the identication and selection process for GxP suppliers ● To create and maintain quality agreement with the GxP supplier ● To assist with oversight of warehouse and distribution business partners by
monitoring compliance with the required standards stipulated in the quality agreement
● To ensure implementation of the SOPs, identify areas of concern and address these with the service providers until resolved.
● Perform audits and assessment of contracted third parties
● To liaise with internal and external stakeholders by providing input on quality standards and procedures, liaising with them on procedures and building skills in the quality standards and procedure requirements as required
**WHO ARE YOU?**
● University degree in one of the following or related science disciplines: pharmacy, medicine, pharmaceutical chemistry and technology, or biology
● 3 - 5 years' experience in pharmaceutical or medical device environment, Regulatory and Quality Assurance Management
● Demonstrate evidence of maintaining and upholding rules and SOP's
Must have knowledge of:
● Current regulatory framework and regulations
● Quality assurance and Quality Management within pharmaceutical environment
● ISO Standards
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
**The Position**
**JOB OBJECTIVE(s):**
To maintain and continuously improve the afliate quality system in compliance with Roche Pharmaceutical Quality System requirements, local GxP-regulations and applicable ISO-standards whilst ensuring an uninterrupted supply of quality products to patients.
**Key Responsibilities**
**●** To conduct regular management review of the QMS by presenting and tracking performance against relevant standards
● To implement quality system in line with ISO/relevant standards by reviewing and understanding divisional SOP, analyse their impact in the local environment and effecting relevant aspects as required
● To identify discrepancies and investigate them via the available quality systems in a timely manner
● To identify and manage changes to processes, persons or systems, evaluate its impact and affected parties, implement planned actions and communicate as required
● To implement local CAPA management by identifying the probable root cause, proposing relevant corrective and/or preventative actions, executing the identied action and evaluating the effectiveness as required
● To conduct quality risk assessments using the quality risk assessment tools , identify risk areas, implementing risk mitigation/elimination measures,and monitor changes as required
● To ensure data integrity by creating, maintaining or implementing relevant SOPs
● To initiate or support quality audits by performing self-inspections, external audits. Identify audit queries, draft audit reports, engage with the relevant parties to implement corrective action and follow up on agreed actions
● To initiate annual mock recall and support actual recall process by informing the Health authority, liaising with the distributor(s) to facilitate product recall, contacting customers and reconciling the returned goods as required
● To maintain up to date knowledge of PQS by participating in physical trainings or provided in virtual learning platforms as required
● To perform training of personnel involved in GxP activities
● To maintain systems for reporting product complaints, including monitoring of the generic product complaints mailbox on business days
● To manage all complaints received based on the the applicable SOP
● Release commercial batches to the local market, and where applicable, Investigation Medicinal Products to the local clinical trial sites, according to the local regulations, Marketing Authorizations and Clinical Trial Authorizations
● To ensure all required KPI's in the product release process are met and feedback is provided as required
● To support the returns process by implementing the relevant SOP, ● Ensure compliance with GDP guidelines and local regulations for the products distributed to the market
● Support batch traceability for all batches received and distributed by the local warehouse
● Coordinate with the supply chain responsible to manage additional controls for cold chain management
● To support the identication and selection process for GxP suppliers ● To create and maintain quality agreement with the GxP supplier ● To assist with oversight of warehouse and distribution business partners by
monitoring compliance with the required standards stipulated in the quality agreement
● To ensure implementation of the SOPs, identify areas of concern and address these with the service providers until resolved.
● Perform audits and assessment of contracted third parties
● To liaise with internal and external stakeholders by providing input on quality standards and procedures, liaising with them on procedures and building skills in the quality standards and procedure requirements as required
**WHO ARE YOU?**
● University degree in one of the following or related science disciplines: pharmacy, medicine, pharmaceutical chemistry and technology, or biology
● 3 - 5 years' experience in pharmaceutical or medical device environment, Regulatory and Quality Assurance Management
● Demonstrate evidence of maintaining and upholding rules and SOP's
Must have knowledge of:
● Current regulatory framework and regulations
● Quality assurance and Quality Management within pharmaceutical environment
● ISO Standards
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
Is this job a match or a miss?
Apply Now
7
Senior Biostatistician - Global BIOS (Permanent Homebased)
Nairobi
IQVIA
Posted 15 days ago
Job Viewed
Job Description
**Join us on our exciting journey!**
The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.
IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.
We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.
**Job Overview:**
As a Senior Biostatistician, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.
You will provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies.
Acting as a statistical team lead for single, complex studies or groups of studies, you will manage the scope of work and budget, providing revenue and resource forecasts, coupled with preparing proposal text and attending bid defense meetings.
You will also collaborate with medical and programming staff to produce interim reports and final reports, allowing a comprehensive understanding and interpretation of the clinical trial data and outcome.
**Requirements:**
+ BSc or MSc degree in Biostatistics or related field and between 4 - 6 years' relevant experience
+ Familiarity with moderately complex statistical methods that apply to applicable clinical trials
+ Good working knowledge of SAS and CDISC SDTM and ADaM
+ Ability to effectively manage multiple tasks and project, ability to communicate and explain statistics
**Join IQVIA to see where your skills can take you**
+ Global exposure
+ Variety of therapeutic areas
+ Collaborative and supportive team environment
+ Access to cutting-edge and innovative, in-house technology
+ Excellent career development and progression opportunities
+ Work-Life Balance, with a strong focus on a positive well-being
**Unleash your potential!**
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.
When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.
IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.
We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.
**Job Overview:**
As a Senior Biostatistician, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas.
You will provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies.
Acting as a statistical team lead for single, complex studies or groups of studies, you will manage the scope of work and budget, providing revenue and resource forecasts, coupled with preparing proposal text and attending bid defense meetings.
You will also collaborate with medical and programming staff to produce interim reports and final reports, allowing a comprehensive understanding and interpretation of the clinical trial data and outcome.
**Requirements:**
+ BSc or MSc degree in Biostatistics or related field and between 4 - 6 years' relevant experience
+ Familiarity with moderately complex statistical methods that apply to applicable clinical trials
+ Good working knowledge of SAS and CDISC SDTM and ADaM
+ Ability to effectively manage multiple tasks and project, ability to communicate and explain statistics
**Join IQVIA to see where your skills can take you**
+ Global exposure
+ Variety of therapeutic areas
+ Collaborative and supportive team environment
+ Access to cutting-edge and innovative, in-house technology
+ Excellent career development and progression opportunities
+ Work-Life Balance, with a strong focus on a positive well-being
**Unleash your potential!**
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.
When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Is this job a match or a miss?
Apply Now
8