What Clinical Project Manager Jobs are in Kenya?
Showing 821 Clinical Project Manager jobs in Kenya
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.**
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0
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
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1
Job Description
About the Role Our client, a pioneering pharmaceutical research organization, is seeking a highly skilled and dedicated Pharmaceutical Research Scientist to contribute to groundbreaking drug discovery and development efforts at their **Kisumu** facility. This position is crucial for advancing our client's pipeline of novel therapeutics. You will be an integral part of a collaborative scientific team, conducting advanced research, analyzing data, and contributing to the publication of scientific findings. The ideal candidate possesses a strong scientific foundation, meticulous attention to detail, and a passion for innovation in pharmaceutical science. This role requires hands-on laboratory work and a commitment to scientific excellence. Join us to make a tangible difference in global health.
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2
Medical Science Liaison (MSL)
00200 Ongata Rongai / Remote
Placements24
Posted 2 days ago
Job Viewed
Job Description
About the Role
Our client, a leading biopharmaceutical company with a strong focus on specialty therapeutics, is seeking an experienced and scientifically driven Medical Science Liaison (MSL) to cover the Ongata Rongai and surrounding regions. This hybrid role requires a deep understanding of a specific therapeutic area and the ability to engage with key opinion leaders (KOLs) and healthcare professionals (HCPs). You will serve as a vital scientific resource, disseminating complex medical information and gathering valuable insights from the medical community. The position involves a mix of remote work for planning and administrative tasks, and significant travel within the territory to meet with KOLs and HCPs.
Key Responsibilities- Establish and maintain peer-to-peer relationships with national and regional KOLs and HCPs within the assigned therapeutic area.
- Present complex scientific and clinical data on company products in a clear and accurate manner.
- Gather and relay important clinical insights, unmet medical needs, and competitive intelligence from the field to internal teams.
- Respond to unsolicited medical information requests from HCPs and support Investigator-Initiated Studies (IIS).
- Collaborate with internal Medical Affairs, Clinical Development, and Commercial teams to ensure alignment of scientific strategies.
- Identify potential investigators for clinical trials and provide scientific support.
- Participate in relevant scientific congresses, advisory boards, and medical education events.
- Develop and deliver scientific presentations and training materials.
- Ensure all activities are conducted in compliance with company policies, industry guidelines, and regulatory requirements.
- Contribute to the development of the regional medical strategy.
- Advanced scientific degree (MD, PharmD, Ph.D.) in a life science or healthcare-related field.
- Minimum of 3-5 years of experience as a Medical Science Liaison or in a similar medical affairs role.
- In-depth knowledge and expertise in a specific therapeutic area relevant to our client's portfolio.
- Proven ability to build and maintain strong relationships with KOLs and HCPs.
- Excellent presentation, communication, and interpersonal skills.
- Strong analytical and critical thinking abilities.
- Ability to work independently and manage travel effectively within a defined territory.
- Proficiency in understanding and interpreting clinical trial data.
- Familiarity with pharmaceutical industry regulations and ethical guidelines.
- Reside within or be willing to relocate to the assigned territory covering Ongata Rongai .
Our client offers a highly competitive salary, bonus structure, and a comprehensive benefits package, including premium health insurance, life insurance, and retirement savings. This hybrid role provides a balance of remote flexibility and the opportunity for impactful field engagement. Opportunities for professional growth and development, including advanced scientific training and leadership programs, are emphasized. Generous paid time off, including annual leave and sick leave, is provided. You will be part of a scientifically focused organization working on innovative treatments that address significant unmet medical needs. A company car, fuel card, and other necessary resources for field activities are provided.
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3
Senior Biostatistician - Global BIOS (Permanent Homebased)
Nairobi
IQVIA
Posted 18 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
4
Job Description
About the Role Our client, a key player in the agricultural processing industry, is seeking an experienced Lead Quality Assurance Specialist for their facility in **Kericho, Kericho, KE**. This hybrid role requires a dedicated professional to lead the quality assurance team and ensure all products meet rigorous quality and safety standards. You will be instrumental in developing, implementing, and maintaining quality management systems, conducting audits, and driving continuous improvement initiatives. The ideal candidate will possess extensive knowledge of quality control methodologies, strong leadership capabilities, and a meticulous attention to detail. You will work closely with production, R&D, and regulatory affairs teams to uphold the highest product integrity. We are looking for a proactive individual who can manage a team, analyze quality data, and implement effective quality assurance strategies to support the company's growth and reputation. Key Responsibilities
- Lead and mentor the quality assurance team, providing guidance and setting performance standards.
- Develop, implement, and maintain robust quality management systems (QMS) and standard operating procedures (SOPs).
- Conduct regular internal audits and inspections to ensure compliance with quality standards and regulations.
- Analyze quality data, identify trends, and recommend corrective and preventive actions (CAPA).
- Collaborate with production and R&D departments to resolve quality issues and improve product consistency.
- Ensure all products meet specified quality parameters and regulatory requirements.
- Oversee the management of non-conforming products and implement appropriate disposition processes.
- Stay updated on industry best practices, regulatory changes, and new quality assurance technologies.
- Train production staff on quality standards and procedures.
- Prepare comprehensive quality reports for management review.
- Bachelor's degree in Food Science, Chemistry, Biology, or a related field.
- Minimum of 6 years of experience in quality assurance or quality control, with at least 2 years in a lead or supervisory role.
- In-depth knowledge of quality management systems (e.g., ISO 9001, HACCP, GMP).
- Strong analytical and problem-solving skills, with the ability to interpret complex data.
- Excellent leadership, communication, and interpersonal skills.
- Experience in the agricultural processing or food manufacturing industry is highly desirable.
- Proficiency in quality control software and data analysis tools.
- Ability to work effectively in both on-site and remote settings as required by the hybrid model.
- Detail-oriented and committed to maintaining the highest quality standards.
- Knowledge of **Kericho, Kericho, KE** regulatory landscape is advantageous.
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5
Senior Clinical Research Associate - Monitoring
20500 Kericho
Placements24
Posted 2 days ago
Job Viewed
Job Description
About the Role
Our client, a dynamic Contract Research Organization (CRO) focused on delivering excellence in clinical trials, is seeking a dedicated Senior Clinical Research Associate (CRA) to join their team in **Kericho**. This is a field-based role requiring significant travel to clinical sites across the region. You will play a critical role in ensuring the quality, integrity, and timely execution of clinical studies by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols and regulatory requirements. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines and extensive experience in clinical trial monitoring. You will be responsible for building strong relationships with investigators and site staff, providing them with necessary training and support. This is an excellent opportunity for an experienced CRA looking to advance their career within a growing organization that values professional development and scientific rigor.
Key Responsibilities- Conduct on-site monitoring visits to clinical trial sites to verify patient safety, data accuracy, and regulatory compliance.
- Initiate, monitor, and close out clinical study sites according to study protocols and standard operating procedures (SOPs).
- Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
- Verify source data and medical records against case report forms (CRFs) for accuracy and completeness.
- Train and provide ongoing support to site staff, including investigators and study coordinators.
- Manage site issues, resolve discrepancies, and implement corrective action plans as needed.
- Oversee drug accountability and ensure proper handling and storage of study materials.
- Prepare visit reports, follow-up letters, and other essential study documentation in a timely manner.
- Participate in site selection and qualification visits as required.
- Contribute to the development and review of study-related documents, including protocols and CRFs.
- Bachelor's degree in a life science, nursing, or a related field. A Master's degree or equivalent is a plus.
- Minimum of 5 years of experience as a Clinical Research Associate, with demonstrated experience in site monitoring.
- Thorough understanding of clinical trial processes, GCP, ICH guidelines, and relevant regulatory requirements.
- Proven ability to conduct effective monitoring visits and manage multiple clinical trial sites simultaneously.
- Excellent interpersonal, communication, and negotiation skills.
- Strong organizational and time management skills, with meticulous attention to detail.
- Ability to travel frequently (up to 75%) to clinical trial sites.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and as part of a team in a demanding environment.
- Commitment to maintaining the highest standards of data integrity and patient safety.
- Competitive salary commensurate with experience.
- Performance-based bonus opportunities.
- Company car or travel allowance.
- Comprehensive health, dental, and vision insurance.
- Paid time off and holidays.
- Opportunities for career advancement and professional development.
- Expense reimbursement for travel and accommodation.
- Retirement savings plan.
- Supportive team environment focused on collaboration.
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6
Job Description
About the Role
Our client is a leading agricultural research institution seeking an experienced Lead Research Scientist specializing in Plant Genetics to join their team in **Meru**. This role offers a hybrid work model, combining remote flexibility with essential on-site laboratory and field activities. You will be responsible for spearheading innovative research projects focused on crop improvement, disease resistance, and yield enhancement through advanced genetic techniques. This position requires a strong background in molecular genetics, plant breeding, and data analysis, with a proven track record of leading research initiatives and publishing scientific findings. You will manage a team of researchers, guide experimental design, and ensure the successful execution of research programs. This is a critical role for driving forward our client's mission to develop sustainable and high-performing crop varieties that address global food security challenges. Your expertise will be vital in shaping the future of agricultural science.
Key Responsibilities- Lead and manage research projects in plant genetics, focusing on areas such as marker-assisted selection, gene editing, and quantitative trait locus (QTL) mapping.
- Design and conduct experiments in both laboratory and field settings to assess genetic variation and performance of crop lines.
- Supervise, mentor, and guide a team of research assistants and junior scientists.
- Analyze large genetic datasets using statistical software and bioinformatics tools.
- Develop and implement breeding strategies for desired traits, including disease resistance and abiotic stress tolerance.
- Collaborate with cross-functional teams, including agronomists, breeders, and biotechnologists.
- Prepare research proposals, secure funding, and manage project budgets.
- Disseminate research findings through publications in peer-reviewed journals and presentations at scientific conferences.
- Ensure compliance with all relevant safety and ethical guidelines in research.
- Ph.D. in Plant Genetics, Molecular Biology, Plant Breeding, or a closely related field.
- Minimum of 7 years of post-doctoral research experience in plant genetics or a related discipline.
- Demonstrated experience in leading research teams and managing complex projects.
- Expertise in molecular marker technologies (e.g., SSRs, SNPs) and next-generation sequencing (NGS) applications in plant science.
- Strong analytical skills with proficiency in statistical analysis software (e.g., R, SAS, GenStat) and bioinformatics tools.
- Experience with plant breeding methodologies and field trial design.
- Excellent communication, interpersonal, and leadership skills.
- Ability to work effectively in a hybrid environment, balancing remote work with on-site laboratory and field activities.
- Publication record in high-impact scientific journals.
- Competitive salary and performance-based bonuses.
- Comprehensive health insurance package.
- Retirement savings plan with employer contribution.
- Generous vacation and sick leave policy.
- Opportunities for international travel and collaboration.
- Access to advanced research facilities and equipment.
- Support for professional development and conference attendance.
- Relocation assistance may be available.
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7
Regulatory Affairs Manager - Pharmaceutical Compliance Lead
30100 Eldoret / Remote
Placements24
Posted 3 days ago
Job Viewed
Job Description
About the Role Our client, a forward-thinking **pharmaceutical** company, is seeking a seasoned Regulatory Affairs Manager to spearhead their regulatory compliance efforts. This is a pivotal, fully remote position, strategically positioned to serve operations and markets connected to **Eldoret, Uasin Gishu, KE**. In this critical role, you will be responsible for navigating the complex regulatory landscape, ensuring that all products meet the stringent requirements set forth by national and international health authorities. You will lead the development and implementation of regulatory strategies, manage submissions, and maintain compliance throughout the product lifecycle. As a remote-first role, we provide a flexible and empowering work environment, equipped with the necessary tools and technology for seamless collaboration with global teams. This opportunity is ideal for a compliance-focused professional seeking to make a substantial impact from a remote setting. Key Responsibilities
- Develop and execute regulatory strategies for product registration and lifecycle management in various markets.
- Prepare, review, and submit regulatory dossiers to health authorities (e.g., NMPA, FDA, EMA).
- Ensure compliance with all relevant national and international pharmaceutical regulations and guidelines.
- Act as the primary point of contact with regulatory agencies and health authorities.
- Monitor changes in the regulatory environment and assess their impact on the company's products and operations.
- Provide regulatory guidance and support to R&D, manufacturing, and commercial teams.
- Oversee the review of labeling, promotional materials, and advertising for regulatory compliance.
- Manage regulatory inspections and audits.
- Contribute to the development and implementation of regulatory policies and procedures.
- Lead and mentor a team of regulatory affairs professionals.
- Master's degree or Ph.D. in Pharmacy, Chemistry, Biology, or a related scientific discipline.
- Minimum of 7 years of progressive experience in regulatory affairs within the **pharmaceutical** industry.
- Proven track record of successfully managing product registrations and regulatory submissions in diverse markets.
- In-depth knowledge of global regulatory requirements, including ICH guidelines.
- Strong understanding of drug development, manufacturing, and quality assurance processes.
- Excellent leadership, project management, and communication skills.
- Ability to think strategically and provide practical solutions to complex regulatory challenges.
- Proficiency in regulatory information management systems.
- Experience working in a remote or hybrid environment is advantageous.
- Must be based in Kenya, with the capacity to work remotely from **Eldoret, Uasin Gishu, KE** or any other suitable location.
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8
Senior AI Research Scientist - Machine Learning Innovation
00100 Machakos / Remote
Placements24
Posted 2 days ago
Job Viewed
Job Description
About the Role Our client, a leading innovator in the AI & Emerging Technologies sector, is seeking a highly skilled and experienced Senior AI Research Scientist to join their dynamic and forward-thinking team. This role is designed for a passionate individual who thrives in a collaborative, fully remote environment and is eager to push the boundaries of machine learning and artificial intelligence. You will be instrumental in developing cutting-edge algorithms and models that address complex real-world challenges. The **Machakos, Machakos, KE**-based role offers a unique opportunity to contribute to groundbreaking research and development, making a significant impact in the field. This position is critical to our client's ongoing success and their commitment to staying at the forefront of technological advancement. We are looking for a self-starter who can work autonomously and contribute meaningfully from day one. Key Responsibilities
- Conduct advanced research in machine learning, deep learning, and related AI fields.
- Design, develop, and implement novel algorithms and models for various applications.
- Collaborate with cross-functional teams to integrate AI solutions into existing and new products.
- Analyze large datasets to extract actionable insights and identify patterns for model improvement.
- Stay abreast of the latest research and industry trends in AI and machine learning.
- Publish research findings in leading academic conferences and journals.
- Mentor junior researchers and contribute to knowledge sharing within the team.
- Develop and maintain high-quality, well-documented code for AI models and experiments.
- Master's or Ph.D. in Computer Science, Artificial Intelligence, Machine Learning, or a related quantitative field.
- Proven track record of research and development in AI/ML, demonstrated through publications or patents.
- Strong proficiency in programming languages such as Python and experience with ML frameworks (e.g., TensorFlow, PyTorch).
- In-depth understanding of various machine learning algorithms, statistical modeling, and data mining techniques.
- Experience with large-scale data processing and distributed computing systems.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong communication and collaboration abilities, essential for a remote work setting.
- Ability to work independently and manage multiple projects simultaneously.
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