134 Clinical Trainee jobs in Kenya
Clinical Manager
Nairobi, Nairobi
Aboosto Group of Comapanies
Posted 11 days ago
Job Viewed
Job Description
Role Summary:
We are seeking an experienced and dynamic Clinic Manager to oversee the day-to-day operations of our aesthetic dermatology clinic. The Clinic Manager will be responsible for ensuring exceptional patient experiences, optimizing operational efficiency, managing clinic staff, and supporting the clinic’s revenue and growth goals. br>Key Responsibilities:
Clinic Operations & Patient Experience
• Oversee all front desk, therapist, and support staff to ensure seamless clinic functioning < r>• nsure high standards of patient service and satisfaction at every touchpoint < r>• M nage clinic scheduling to minimize waiting time and optimize productivity < r>• H ndle client grievances professionally and ensure timely resolution < r>Revenue & Business Development
• M nitor daily, weekly, and monthly sales targets and clinic performance metrics < r>• I plement strategies to increase patient retention, upselling, and new client acquisition < r>• C llaborate with the marketing team on promotional campaigns, events, and social media initiatives < r>• S pport doctors and therapists in converting consultations to treatments < r>Team Leadership & HR Coordination
• S pervise, train, and evaluate staff performance regularly < r>• C nduct daily briefings, maintain staff discipline, and resolve internal conflicts < r>• E sure adherence to clinic policies, grooming standards, and attendance discipline < r>• C ordinate recruitment needs, onboarding, and performance appraisals in consultation with HR < r> Inventory & Compliance Management
• M nitor stock levels for skincare products, consumables, and medical equipment < r>• E sure timely ordering, usage tracking, and inventory reconciliation < r>• M intain hygiene, safety, and regulatory compliance (clinical waste, SOPs, audits) < r>• E sure equipment is maintained and service contracts are up to date < r>
Qualifications & Experience:
• B chelor's degree in Healthcare Management / Business Administration / Hospitality < r>• M nimum 3–5 years’ experience in managing aesthetic, dermatology, or wellness clinics
• Familiarity with clinic software (EMR, CRM, billing)
• Strong nderstanding of dermatology/cosmetic treatments is an advantage
We are seeking an experienced and dynamic Clinic Manager to oversee the day-to-day operations of our aesthetic dermatology clinic. The Clinic Manager will be responsible for ensuring exceptional patient experiences, optimizing operational efficiency, managing clinic staff, and supporting the clinic’s revenue and growth goals. br>Key Responsibilities:
Clinic Operations & Patient Experience
• Oversee all front desk, therapist, and support staff to ensure seamless clinic functioning < r>• nsure high standards of patient service and satisfaction at every touchpoint < r>• M nage clinic scheduling to minimize waiting time and optimize productivity < r>• H ndle client grievances professionally and ensure timely resolution < r>Revenue & Business Development
• M nitor daily, weekly, and monthly sales targets and clinic performance metrics < r>• I plement strategies to increase patient retention, upselling, and new client acquisition < r>• C llaborate with the marketing team on promotional campaigns, events, and social media initiatives < r>• S pport doctors and therapists in converting consultations to treatments < r>Team Leadership & HR Coordination
• S pervise, train, and evaluate staff performance regularly < r>• C nduct daily briefings, maintain staff discipline, and resolve internal conflicts < r>• E sure adherence to clinic policies, grooming standards, and attendance discipline < r>• C ordinate recruitment needs, onboarding, and performance appraisals in consultation with HR < r> Inventory & Compliance Management
• M nitor stock levels for skincare products, consumables, and medical equipment < r>• E sure timely ordering, usage tracking, and inventory reconciliation < r>• M intain hygiene, safety, and regulatory compliance (clinical waste, SOPs, audits) < r>• E sure equipment is maintained and service contracts are up to date < r>
Qualifications & Experience:
• B chelor's degree in Healthcare Management / Business Administration / Hospitality < r>• M nimum 3–5 years’ experience in managing aesthetic, dermatology, or wellness clinics
• Familiarity with clinic software (EMR, CRM, billing)
• Strong nderstanding of dermatology/cosmetic treatments is an advantage
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0
Clinical Aesthetician
20100 Mwembe
KES120000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client is seeking a talented and compassionate Clinical Aesthetician to join their fully remote wellness team. This position focuses on providing expert skincare consultations and treatment plan recommendations through virtual platforms. The ideal candidate will have a strong background in dermatology and a passion for enhancing clients' skin health and appearance, delivered entirely from a remote setting.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct thorough virtual skin analysis and consultations with clients.
- Develop personalized skincare treatment plans based on individual client needs and concerns.
- Educate clients on proper skincare routines, product usage, and ingredient benefits.
- Recommend and advise on appropriate aesthetic treatments and product lines.
- Maintain detailed client records and track progress over time through virtual check-ins.
- Stay updated on the latest advancements in skincare, treatments, and technologies.
- Provide excellent customer service and build strong client relationships remotely.
- Collaborate with other wellness professionals within the organization to offer holistic care.
- Ensure client privacy and confidentiality are maintained at all times.
- Achieve client satisfaction and retention goals through exceptional service.
Qualifications:
- Certified Aesthetician with a recognized qualification.
- Minimum of 4 years of hands-on experience as an aesthetician, preferably with a focus on clinical treatments.
- Strong knowledge of dermatology, skin physiology, and various skincare concerns.
- Experience with virtual consultations and client management software.
- Excellent communication, interpersonal, and active listening skills, crucial for remote interaction.
- Proficiency in using digital tools for client assessment and record-keeping.
- Aesthetician license and relevant certifications.
- Ability to work independently and manage time effectively in a remote environment.
- A genuine passion for skincare and client well-being.
- Understanding of cosmetic ingredients and their effects on the skin.
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1
Clinical Pharmacologist
60100 Embu, Eastern
KES320000 Annually
WhatJobs
Posted 2 days ago
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Job Description
Our client, a leading biopharmaceutical company, is seeking a highly qualified Clinical Pharmacologist to join their expanding research department. This is a fully remote position, offering the flexibility to contribute from anywhere. The successful candidate will be instrumental in designing and executing clinical trials, analyzing pharmacokinetic and pharmacodynamic data, and providing scientific expertise to support drug development programs. Your responsibilities will include developing clinical pharmacology strategies, writing protocols and study reports, and ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. You will work closely with clinical operations, biostatistics, and regulatory affairs teams to advance drug candidates through the development pipeline. A deep understanding of drug metabolism, transport, and interactions is essential, as is the ability to interpret complex clinical data and translate it into actionable insights. You will contribute to regulatory submissions and interact with health authorities as needed. The ideal candidate possesses strong analytical skills, meticulous attention to detail, and excellent written and verbal communication abilities. Experience with modeling and simulation techniques (e.g., NONMEM) is highly desirable. This role demands a proactive approach, the ability to manage multiple projects concurrently, and a commitment to scientific excellence. We are looking for an individual passionate about improving patient outcomes through innovative medicines. Join our client's dedicated team and play a critical role in bringing life-changing therapies to patients worldwide, all while enjoying the benefits of a remote work environment.
Responsibilities:
Qualifications:
Responsibilities:
- Develop clinical pharmacology strategies for drug development programs.
- Design and write clinical trial protocols and study reports.
- Analyze pharmacokinetic (PK) and pharmacodynamic (PD) data.
- Provide scientific input for regulatory submissions.
- Collaborate with clinical operations, biostatistics, and regulatory teams.
- Ensure compliance with GCP and relevant regulatory guidelines.
- Contribute to the interpretation of clinical trial results.
- Support drug metabolism and pharmacokinetic studies.
- Prepare and review study documents and publications.
- Participate in interactions with health authorities.
Qualifications:
- Ph.D. or Pharm.D. with a specialization in Clinical Pharmacology or a related field.
- Minimum of 4 years of experience in clinical pharmacology within the pharmaceutical or biotechnology industry.
- Strong knowledge of PK/PD principles and modeling/simulation techniques.
- Experience with regulatory guidelines (e.g., FDA, EMA) and GCP.
- Proficiency in data analysis software (e.g., Phoenix WinNonlin, NONMEM).
- Excellent scientific writing and communication skills.
- Ability to work independently and manage projects in a remote setting.
- Strong analytical and problem-solving abilities.
- Experience in specific therapeutic areas is a plus.
- Team player with a collaborative spirit.
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2
Clinical Research Associate
80101 Nairobi, Nairobi
KES95000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical entity, is actively seeking a dedicated and experienced Clinical Research Associate (CRA) to join their fully remote global team. This critical role will involve the oversight and management of clinical trials, ensuring adherence to protocols, regulations, and ethical standards. You will be responsible for site selection, initiation, monitoring, and close-out activities. Your primary objective will be to ensure the quality, integrity, and accuracy of the data collected during clinical studies, which are vital for the development of new pharmaceuticals. This position requires extensive travel to study sites when necessary, but the core administrative and planning functions are performed remotely. Key responsibilities include:
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is a plus. A minimum of 3-5 years of direct experience as a CRA is required, with a strong understanding of clinical trial phases and methodologies. Excellent knowledge of ICH-GCP guidelines and regulatory affairs is essential. Superior organizational skills, meticulous attention to detail, and strong written and verbal communication abilities are paramount. You must be proficient in clinical trial management systems (CTMS) and electronic data capture (EDC) systems. The ability to work independently, manage your time effectively, and travel as needed is crucial for success in this remote-first role. This is an exceptional opportunity to contribute to life-saving medical advancements from the comfort of your home office, with necessary travel to research locations. We are looking for passionate professionals committed to advancing healthcare through rigorous clinical research. Join our client's esteemed research division.
- Identifying and qualifying potential clinical trial sites.
- Conducting pre-study, initiation, monitoring, and close-out visits.
- Ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Monitoring study conduct, data collection, and patient safety.
- Verifying source data and ensuring its accuracy against the case report forms (CRFs).
- Managing communication between the sponsor and clinical sites.
- Resolving site-level issues and ensuring timely data entry and query resolution.
- Training site personnel on study protocols and procedures.
- Preparing monitoring reports and ensuring all study documentation is accurate and complete.
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is a plus. A minimum of 3-5 years of direct experience as a CRA is required, with a strong understanding of clinical trial phases and methodologies. Excellent knowledge of ICH-GCP guidelines and regulatory affairs is essential. Superior organizational skills, meticulous attention to detail, and strong written and verbal communication abilities are paramount. You must be proficient in clinical trial management systems (CTMS) and electronic data capture (EDC) systems. The ability to work independently, manage your time effectively, and travel as needed is crucial for success in this remote-first role. This is an exceptional opportunity to contribute to life-saving medical advancements from the comfort of your home office, with necessary travel to research locations. We are looking for passionate professionals committed to advancing healthcare through rigorous clinical research. Join our client's esteemed research division.
This advertiser has chosen not to accept applicants from your region.
3
Senior Clinical Aesthetician
00300 Kitale, Rift Valley
KES95000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client is looking for a highly skilled and experienced Senior Clinical Aesthetician to lead our fully remote team. This is a unique opportunity to provide expert skincare consultations and treatment recommendations remotely, guiding clients through personalized wellness journeys. You will leverage your in-depth knowledge of skin physiology, cosmetic ingredients, and advanced aesthetic treatments to deliver exceptional client care from the comfort of your home. Responsibilities include conducting virtual skin analysis, developing customized treatment plans, and educating clients on skincare routines and product usage. You will also be responsible for staying updated on the latest trends and technologies in the beauty and wellness industry, as well as contributing to content creation for client education. A strong understanding of dermatology, corrective skincare, and non-invasive treatments is essential. Excellent communication and interpersonal skills are paramount for building rapport with clients and providing a high level of service. You will work with a diverse clientele, offering tailored advice and support. The ideal candidate is passionate about holistic beauty, possesses a keen eye for detail, and is adept at problem-solving in a remote environment. This role demands a self-starter attitude, strong organizational skills, and the ability to manage client relationships effectively. You will be instrumental in enhancing client satisfaction and driving engagement with our innovative wellness programs.
Key Responsibilities:
Key Responsibilities:
- Conduct comprehensive virtual skin consultations and analysis.
- Develop personalized skincare and treatment plans for clients.
- Educate clients on proper skincare techniques and product selection.
- Provide remote guidance on advanced aesthetic procedures.
- Stay current with industry trends, product innovations, and emerging technologies.
- Create educational content for clients, such as articles and videos.
- Manage client appointments and follow-ups efficiently.
- Maintain client records and track progress remotely.
- Collaborate with other remote team members to enhance client experience.
- Certified Aesthetician or equivalent professional qualification.
- Minimum of 4 years of experience in a clinical aesthetic setting.
- In-depth knowledge of skin biology, cosmetic ingredients, and treatment modalities.
- Experience with virtual client consultations and telehealth platforms.
- Excellent communication, empathy, and client service skills.
- Ability to work autonomously and manage time effectively in a remote setting.
- Proficiency in skincare analysis tools and digital platforms.
- A passion for the beauty and wellness industry and continuous learning.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
40100 Kisumu
KES190000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client is seeking a detail-oriented and experienced Clinical Research Associate to join their vital pharmaceutical research team. This is a fully remote role, offering a critical opportunity to contribute to groundbreaking drug development from your home office. You will be responsible for monitoring clinical trials, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your duties will include site initiation visits, regular site monitoring, and close-out visits, all conducted remotely or with minimal travel as per trial requirements. You will review and verify case report forms (CRFs), source documents, and ensure the accuracy and completeness of trial data. This role demands a thorough understanding of clinical trial processes, therapeutic areas, and regulatory landscapes. The ideal candidate will possess a bachelor's degree in a life science, nursing, or a related field, with a minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role. Strong knowledge of ICH-GCP guidelines and regulatory requirements (e.g., FDA, EMA) is essential. Excellent communication, organizational, and data management skills are required, along with the ability to work independently and manage multiple priorities. This is an exceptional opportunity to advance your career in the pharmaceutical industry, working on cutting-edge research with a company that values scientific integrity and employee well-being, offering a competitive salary and the convenience of a remote work environment. Your meticulous approach will ensure the integrity and reliability of clinical trial data, directly contributing to patient safety and the development of new medicines.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate
00100 Abothuguchi West
KES120000 month
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their dynamic team in **Nairobi, Nairobi, KE**. This role is critical for the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and good clinical practices (GCP). As a CRA, you will be responsible for monitoring clinical trial sites, verifying data accuracy, ensuring patient safety, and maintaining essential trial documentation. You will build strong relationships with investigators and site staff, providing guidance and support throughout the trial process. The ideal candidate will have a Bachelor's degree in a life science or healthcare-related field, coupled with significant experience as a CRA or in a similar clinical research role. Strong knowledge of GCP, clinical trial processes, and regulatory guidelines is essential. Excellent organizational, communication, and interpersonal skills are vital for this position. You must be adept at managing multiple sites and projects, demonstrating a high level of accuracy and attention to detail. This is an excellent opportunity for a motivated professional to contribute to life-saving medical advancements within a reputable organization. Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with study protocols, SOPs, and GCP.
- Verify the accuracy, completeness, and integrity of clinical data.
- Ensure patient safety and timely reporting of adverse events.
- Conduct site initiation, interim monitoring, and close-out visits.
- Train and support investigators and site staff on study-related procedures.
- Maintain accurate and complete trial master files (TMF) and site files.
- Liaise with study sponsors, CROs, and regulatory authorities.
- Resolve data queries and ensure timely data entry.
- Prepare monitoring reports and communicate findings to the study team.
- Ensure compliance with all applicable regulatory requirements and company policies.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 3-5 years of experience as a Clinical Research Associate or similar role.
- In-depth knowledge of ICH-GCP guidelines and clinical trial regulations.
- Experience in site monitoring and data verification.
- Excellent understanding of clinical trial processes from initiation to close-out.
- Strong organizational, time management, and problem-solving skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent written and verbal communication skills.
- Ability to travel to clinical trial sites as required.
- Strong ethical conduct and attention to detail.
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6
Clinical Research Associate
70100 Moiben
KES70000 month
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client is looking for an experienced Clinical Research Associate to support their pharmaceutical research and development efforts. This role, based in **Garissa, Garissa, KE**, will involve direct involvement in clinical trials, ensuring compliance with protocols and regulatory standards. The successful candidate will be responsible for site monitoring, data collection, and ensuring the integrity and accuracy of trial information. Key duties include recruiting and enrolling study participants, conducting patient visits, administering study-related procedures, and managing study documentation. You will also be responsible for maintaining communication with investigators, study staff, and the sponsor to ensure smooth trial operations. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. A Bachelor's degree in a life science or healthcare-related field, or equivalent experience, is required. Prior experience as a Clinical Research Coordinator or Associate is highly preferred. Excellent organizational skills, meticulous attention to detail, and strong interpersonal and communication abilities are essential for success in this position. You will play a critical role in advancing pharmaceutical research and bringing new treatments to patients, contributing significantly to our client's mission. This role offers a hybrid work arrangement, balancing on-site responsibilities with remote flexibility.
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7
Clinical Research Associate
50101 Kakamega, Western
KES110000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a dynamic pharmaceutical company committed to advancing global health, is seeking an experienced Clinical Research Associate (CRA) to join their fully remote clinical operations team. This position is integral to the successful management and execution of clinical trials, ensuring compliance with protocols and regulatory requirements. The CRA will be responsible for site selection and initiation, monitoring study progress, ensuring data integrity, and supporting site staff through remote interactions. Key responsibilities include performing remote site visits and monitoring, reviewing essential documents, managing study timelines, and communicating effectively with investigators, study coordinators, and internal project teams. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines, clinical trial management, and regulatory affairs within the pharmaceutical industry. Previous experience as a CRA or in a similar role within clinical research is essential. Excellent organizational, analytical, and problem-solving skills are required, along with exceptional communication and interpersonal abilities to foster strong relationships remotely. This fully remote role offers the flexibility to work from home and contribute to impactful medical research, supporting trials that may have operational links to **Kakamega, Kakamega, KE**, necessitating remote oversight and data management.
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8
Clinical Research Associate
00200 Moiben
KES15000 Daily
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and experienced Clinical Research Associate (CRA) to join their team in Garissa, Garissa . This hybrid role involves a mix of remote work and on-site visits to clinical trial sites. As a CRA, you will be responsible for monitoring the progress of clinical trials, ensuring that they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. You will play a pivotal role in managing site activities, training site staff, and ensuring data accuracy and patient safety. This is a critical position that requires meticulous attention to detail, strong organizational skills, and the ability to build effective relationships with investigators and study staff. You will travel to investigational sites to verify that all study procedures are being followed correctly and that all necessary documentation is in place. The role demands a comprehensive understanding of regulatory requirements and a proactive approach to problem-solving. Successful candidates will be adept at identifying and addressing any deviations from the protocol or regulatory standards. This is an excellent opportunity for a skilled CRA to contribute to life-saving research within a supportive and growth-oriented environment. If you are passionate about pharmaceutical research, possess excellent interpersonal skills, and are committed to upholding the highest standards of clinical trial conduct, we encourage you to apply.
Responsibilities:
Qualifications:
Responsibilities:
- Initiate, monitor, and close-out clinical trial sites.
- Ensure compliance with protocols, SOPs, and GCP guidelines.
- Verify the accuracy and completeness of study data.
- Manage and train site personnel on study requirements.
- Oversee drug accountability and investigational product management.
- Conduct site visits (remote and on-site) as per the monitoring plan.
- Resolve data queries and address protocol deviations.
- Communicate effectively with study teams, investigators, and regulatory authorities.
- Prepare and submit monitoring visit reports.
- Ensure timely submission of essential documents.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Proven experience in clinical trial monitoring and site management.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Proficiency in clinical trial management software.
- Ability to travel as required.
- Detail-oriented with strong analytical skills.
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