1,423 Clinical Scientist jobs in Kenya
Lead Clinical Research Scientist
50100 Kitale, Rift Valley
KES380000 Annually
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Our client, a cutting-edge research institution, is seeking a Lead Clinical Research Scientist to drive impactful studies in groundbreaking scientific fields. This is a fully remote opportunity, enabling collaboration with global research teams. You will be responsible for designing, implementing, and managing clinical research protocols, analyzing study data, and contributing to the dissemination of research findings. Key responsibilities include developing hypotheses, overseeing patient recruitment and data collection, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams of scientists, clinicians, and statisticians. The ideal candidate will possess a Ph.D. or Master's degree in a relevant scientific discipline (e.g., Biology, Chemistry, Pharmacology, Medical Science) and a minimum of 8 years of experience in clinical research, with a proven track record of leadership in research projects. Experience with clinical trial management systems, data analysis software (e.g., R, SPSS), and a deep understanding of research methodologies and ethical considerations are essential. Strong analytical, problem-solving, and scientific writing skills are crucial. You should be adept at leading research teams, securing funding, and presenting complex scientific information to diverse audiences. This role offers an exceptional opportunity to contribute to advancements in science and medicine.
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0
Senior Clinical Research Scientist
30300 Kitale, Rift Valley
KES800000 Annually
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Our client, a pioneering firm in Scientific Research & Development, is seeking an experienced Senior Clinical Research Scientist to lead critical research initiatives within their fully remote team. This vital role involves the design, execution, and analysis of clinical trials, contributing to the advancement of novel therapies and technologies. You will be responsible for developing study protocols, overseeing patient recruitment, managing data collection and analysis, and ensuring compliance with all regulatory standards and ethical guidelines. The successful candidate will possess a strong scientific background, extensive knowledge of clinical trial methodologies, and experience with statistical analysis software. Excellent written and verbal communication skills are essential for preparing scientific publications, presenting findings at conferences, and collaborating with regulatory bodies and research partners. You will also mentor junior research staff and contribute to the strategic direction of research programs. The ability to manage complex projects, critically evaluate scientific data, and thrive in a fast-paced, remote research environment is paramount. Proficiency with research databases, scientific literature review tools, and virtual collaboration platforms is required. This is an exceptional opportunity to make a significant impact on scientific discovery and patient care from a remote setting.
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1
Clinical Research Scientist - Oncology
40100 Kisumu
KES400000 Annually
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Our client, a pioneering pharmaceutical company dedicated to advancing global health, is actively seeking a highly qualified Clinical Research Scientist specializing in Oncology to join their fully remote research and development team. This critical role will involve the design, execution, and analysis of clinical trials for novel cancer therapies. You will be responsible for developing clinical trial protocols, identifying suitable investigators and research sites, and overseeing the conduct of studies in compliance with regulatory guidelines (e.g., ICH-GCP). Your expertise will be vital in analyzing clinical data, interpreting results, and contributing to regulatory submissions and scientific publications. This position demands a rigorous scientific approach, meticulous attention to detail, and a deep understanding of oncology drug development. You will collaborate closely with internal teams, including R&D, regulatory affairs, and medical affairs, as well as external partners, including academic institutions and contract research organizations (CROs). The ability to effectively communicate complex scientific information to diverse audiences is paramount. This is an outstanding opportunity to contribute to life-changing research in a remote-first environment, working with a team committed to innovation and patient well-being. You will play a key role in bringing new treatments to patients who need them most. Our client fosters a culture of scientific excellence and offers extensive opportunities for professional development. Join us and be at the forefront of cancer research.
Responsibilities:
Qualifications:
Responsibilities:
- Design and develop clinical trial protocols for oncology therapies.
- Oversee the operational execution of clinical trials, ensuring adherence to protocols and GCP.
- Monitor study progress, manage data collection, and analyze study results.
- Contribute to the preparation of clinical study reports (CSRs) and regulatory submissions.
- Collaborate with investigators, research staff, and CROs to ensure quality data.
- Evaluate and interpret clinical trial data, identifying trends and key findings.
- Provide scientific and technical guidance to project teams.
- Stay updated on the latest advancements in oncology and clinical research.
- Contribute to the development of new drug candidates and treatment strategies.
- Present research findings at scientific conferences and in peer-reviewed journals.
Qualifications:
- Ph.D. or M.D. in a relevant life science field (e.g., Oncology, Pharmacology, Immunology).
- Extensive experience in clinical research, with a strong focus on oncology trials.
- In-depth knowledge of drug development processes and regulatory requirements.
- Proven ability to design, manage, and analyze clinical trials.
- Excellent scientific writing and presentation skills.
- Strong understanding of statistical analysis principles in clinical research.
- Ability to work independently and collaboratively in a remote setting.
- Demonstrated problem-solving skills and critical thinking.
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2
Senior Clinical Research Scientist - Oncology
40100 Kisumu
KES200000 Annually
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Our client is seeking a highly accomplished and motivated Senior Clinical Research Scientist specializing in Oncology to join their pioneering, fully remote research and development team. This role is crucial for designing, executing, and analyzing groundbreaking clinical trials aimed at developing novel cancer therapies. You will lead cross-functional teams, manage study protocols, interpret complex data sets, and contribute significantly to regulatory submissions. The ideal candidate will possess a deep understanding of oncology, clinical trial methodologies, and biostatistics.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop clinical trial protocols for oncology studies, ensuring scientific rigor and regulatory compliance.
- Oversee the execution of clinical trials, including site selection, patient recruitment, data collection, and monitoring.
- Analyze and interpret complex clinical trial data, including efficacy, safety, and pharmacokinetic data.
- Prepare high-quality clinical study reports, manuscripts for publication, and regulatory submission documents.
- Collaborate with statisticians, data managers, and medical monitors to ensure data integrity and accurate analysis.
- Lead cross-functional teams, including clinical research associates (CRAs), medical affairs, and regulatory affairs personnel.
- Stay abreast of the latest advancements in oncology research, clinical trial design, and regulatory guidelines.
- Identify and evaluate new therapeutic targets and drug candidates for clinical development.
- Present research findings at scientific conferences and to internal stakeholders.
- Manage relationships with external collaborators, key opinion leaders (KOLs), and contract research organizations (CROs).
- Contribute to the strategic planning and pipeline development for the oncology portfolio.
- Ensure all research activities are conducted in accordance with Good Clinical Practice (GCP) guidelines and relevant regulations.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology).
- Minimum of 7 years of experience in clinical research, with a significant focus on oncology drug development.
- Proven experience in designing and managing Phase I, II, and III clinical trials.
- Strong understanding of oncology disease states, molecular mechanisms, and therapeutic strategies.
- Expertise in statistical analysis methods and interpretation of clinical trial data.
- Excellent written and verbal communication skills, with a strong publication record.
- Demonstrated leadership and project management capabilities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work effectively in a fast-paced, remote, and collaborative research environment.
- Deep understanding of regulatory requirements (e.g., FDA, EMA).
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3
Lead Clinical Research Scientist (Remote)
20200 Kapsuser
KES300000 Annually
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Our client, a cutting-edge biotechnology firm, is actively seeking a highly accomplished Lead Clinical Research Scientist to spearhead groundbreaking research initiatives. This position is entirely remote, offering the flexibility to work from anywhere. As the Lead Clinical Research Scientist, you will play a pivotal role in designing, executing, and analyzing complex scientific studies, contributing significantly to the development of novel therapeutic agents. Your responsibilities will encompass leading cross-functional research teams, developing innovative research methodologies, and ensuring the rigorous application of scientific principles throughout the research lifecycle. You will be expected to author protocols, interpret complex data sets, and contribute to the preparation of scientific publications and regulatory submissions.
This role demands a deep understanding of clinical trial design, statistical analysis, and regulatory guidelines pertinent to drug development. You will be responsible for mentoring junior scientists, fostering a collaborative and intellectually stimulating remote research environment, and staying abreast of the latest advancements in your field. The ideal candidate will possess a strong publication record, excellent critical thinking skills, and a proven ability to manage multiple research projects simultaneously. Experience with molecular biology techniques, preclinical studies, and translational research is highly desirable. Your expertise will be crucial in guiding the company's research strategy and driving the successful translation of scientific discoveries into tangible clinical outcomes.
Qualifications:
This role demands a deep understanding of clinical trial design, statistical analysis, and regulatory guidelines pertinent to drug development. You will be responsible for mentoring junior scientists, fostering a collaborative and intellectually stimulating remote research environment, and staying abreast of the latest advancements in your field. The ideal candidate will possess a strong publication record, excellent critical thinking skills, and a proven ability to manage multiple research projects simultaneously. Experience with molecular biology techniques, preclinical studies, and translational research is highly desirable. Your expertise will be crucial in guiding the company's research strategy and driving the successful translation of scientific discoveries into tangible clinical outcomes.
Qualifications:
- Ph.D. in Biology, Biochemistry, Pharmacology, or a related life science discipline.
- Minimum of 10 years of post-doctoral research experience in a relevant scientific field, with at least 3 years in a leadership or principal investigator role.
- Extensive experience in designing and conducting clinical research studies.
- Proficiency in statistical analysis software (e.g., R, SAS) and data interpretation.
- Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory affairs (e.g., FDA, EMA).
- Proven ability to lead and mentor scientific teams.
- Excellent written and verbal communication skills, with a track record of scientific publications.
- Demonstrated ability to secure research funding (grant writing experience is a plus).
- Exceptional problem-solving skills and attention to detail in a remote setting.
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4
Senior Clinical Safety Scientist
30100 Moiben
KES430000 Annually
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Our client, a leading pharmaceutical company dedicated to improving global health, is seeking a highly experienced Senior Clinical Safety Scientist to strengthen its pharmacovigilance operations. This position is fully remote, offering the flexibility to contribute from anywhere. The ideal candidate will possess extensive expertise in clinical trial safety, signal detection, and regulatory reporting, ensuring the safety and well-being of patients participating in clinical studies.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Manage and oversee the safety surveillance activities for assigned clinical trials, ensuring adherence to Good Clinical Practice (GCP) and regulatory requirements.
- Review and analyze adverse event data from clinical studies, identifying potential safety signals and trends.
- Prepare and submit expedited safety reports and periodic safety update reports to regulatory authorities and ethics committees.
- Collaborate closely with clinical operations, data management, and regulatory affairs teams to ensure timely and accurate safety reporting.
- Develop and implement safety monitoring plans and risk management strategies for clinical trials.
- Conduct literature reviews and database searches to identify and evaluate potential safety concerns.
- Ensure the integrity and accuracy of safety data within clinical trial databases and safety reporting systems.
- Contribute to the development and review of clinical trial protocols and investigator brochures regarding safety information.
- Provide expert input on safety-related matters during study initiation, conduct, and close-out phases.
- Train and mentor junior safety scientists and clinical site staff on safety reporting procedures.
- Participate in cross-functional safety review meetings and contribute to informed decision-making regarding product safety.
Qualifications:
- Master's degree or higher in a healthcare-related field (e.g., Medicine, Pharmacy, Nursing, Public Health).
- Minimum of 5-7 years of experience in clinical trial safety, pharmacovigilance, or a related drug safety role.
- In-depth knowledge of clinical trial processes and ICH guidelines, particularly those related to safety reporting.
- Proven experience in identifying, assessing, and reporting adverse events and serious adverse events.
- Familiarity with safety databases and electronic data capture (EDC) systems used in clinical trials.
- Excellent analytical, critical thinking, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to clearly articulate complex safety information.
- Demonstrated ability to work independently, manage multiple clinical studies, and meet strict deadlines in a remote setting.
- Proficiency in relevant software applications and data analysis tools.
- Strong understanding of regulatory requirements for safety reporting in different global regions.
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5
Remote Senior Clinical Research Scientist - Oncology
20200 Kapsuser
KES5000 Hourly
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Our client is a premier clinical research organization seeking a highly accomplished Remote Senior Clinical Research Scientist specializing in Oncology. This fully remote position demands expertise in designing, executing, and managing early-phase oncology clinical trials. You will be responsible for developing study protocols, managing data integrity, and collaborating with investigators and clinical sites globally through virtual channels. This role is crucial for advancing novel cancer therapies from the laboratory to clinical application. Key responsibilities include the development and writing of clinical trial protocols, Investigator's Brochures, and informed consent forms. You will oversee the selection and activation of clinical trial sites, ensuring investigators and study staff are adequately trained on study procedures and regulatory requirements. Monitoring study progress, ensuring adherence to protocols and regulatory guidelines (e.g., GCP, ICH), and managing data collection and analysis are paramount. You will work closely with biostatisticians and data managers to ensure data quality and integrity. Furthermore, you will actively participate in scientific discussions, contribute to regulatory submissions, and present study findings at virtual scientific meetings. Essential qualifications include a Ph.D. or MD with a minimum of 7 years of experience in clinical research, with at least 4 years focused specifically on oncology clinical trials. A strong understanding of cancer biology, drug development processes, and regulatory affairs is mandatory. Proven experience in protocol design, clinical operations, and data analysis for oncology studies is required. Excellent written and verbal communication skills are essential for authoring complex scientific documents and presenting findings. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant software is necessary. The ability to work independently, manage multiple projects, and lead virtual teams effectively is critical. This is a fully remote position, providing an exceptional opportunity to contribute to life-changing cancer research from a flexible work environment. You will be an integral part of a leading scientific team, driving innovation in cancer treatment. The role requires a strategic thinker with a deep commitment to scientific rigor and patient well-being. Your scientific leadership will support research initiatives relevant to areas near Kericho, Kericho, KE , although the role is conducted entirely remotely.
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6
Senior Medical Research Scientist
80100 Nairobi, Nairobi
KES490000 Annually
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Our client is a leading medical research institution seeking a highly accomplished Senior Medical Research Scientist to lead groundbreaking studies. This is a fully remote position, allowing you to contribute to vital medical advancements from anywhere. You will be responsible for designing, executing, and analyzing complex research projects, focusing on developing innovative diagnostics, therapeutics, or understanding disease mechanisms. Your role will involve conceptualizing research hypotheses, designing experimental methodologies, collecting and analyzing data, and interpreting results to contribute to significant scientific discoveries. Collaboration with a multidisciplinary team of clinicians, biologists, statisticians, and other researchers is crucial. You will also be expected to write grant proposals, publish findings in high-impact journals, and present at national and international conferences. The ideal candidate will possess a Ph.D. in a relevant biomedical or life sciences field, a strong publication record, and extensive experience in designing and conducting clinical or laboratory-based research. Expertise in specific medical research areas, advanced statistical analysis, and data interpretation skills are essential. This role offers an exceptional opportunity to shape the future of healthcare through impactful research, working flexibly within a global team, contributing to research initiatives connected to **Mombasa, Mombasa, KE**.
Key Responsibilities:
Key Responsibilities:
- Conceptualize, design, and execute complex medical research projects.
- Develop and validate research methodologies and experimental protocols.
- Collect, manage, and analyze large-scale biological and clinical data.
- Interpret research findings and draw meaningful conclusions.
- Write grant proposals to secure funding for research initiatives.
- Prepare manuscripts for publication in peer-reviewed scientific journals.
- Present research findings at scientific conferences and meetings.
- Collaborate with a multidisciplinary team of scientists, clinicians, and technicians.
- Mentor and guide junior research staff and students.
- Ensure research is conducted ethically and in compliance with all regulations.
- Stay abreast of the latest advancements and discoveries in medical research.
- Contribute to the strategic direction of the research department.
- Ph.D. in Biomedical Sciences, Medicine, Biology, Pharmacology, or a related field.
- Minimum of 8 years of postdoctoral research experience in a medical or scientific setting.
- Proven track record of leading successful research projects and securing grant funding.
- Strong publication record in reputable scientific journals.
- Expertise in designing and conducting laboratory-based or clinical research.
- Advanced knowledge of statistical analysis and data interpretation techniques.
- Familiarity with research methodologies, scientific instrumentation, and data management tools.
- Excellent analytical, critical thinking, and problem-solving skills.
- Exceptional written and verbal communication skills for scientific reporting and presentations.
- Ability to work independently and lead research teams effectively in a remote environment.
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7
Clinical Research Associate
80101 Nairobi, Nairobi
KES95000 Annually
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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.
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8
Clinical Research Associate
40100 Kisumu
KES190000 Annually
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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.
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