3,096 Clinical Research jobs in Kenya
Clinical Research Scientist
20100 Nyeri Town
KES5500000 Annually
WhatJobs
Posted 7 days ago
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Job Description
Our client, a leading innovator in the pharmaceutical sector, is looking for a dedicated and experienced Clinical Research Scientist to join their globally distributed team. This is a fully remote position, allowing you to contribute from the comfort of your own home, ideally located within or with strong connectivity to Nyeri, Nyeri, KE , though geographical boundaries are flexible for the right candidate. You will be instrumental in the design, execution, and analysis of clinical trials, playing a pivotal role in bringing life-changing medications to market. Responsibilities include developing clinical trial protocols, selecting and monitoring clinical investigator sites, ensuring compliance with regulatory guidelines (e.g., GCP, ICH), managing data collection and analysis, and preparing scientific reports and publications. You will collaborate closely with cross-functional teams, including statisticians, medical writers, regulatory affairs, and R&D departments, often in a virtual environment. The ideal candidate will possess a strong scientific background, excellent understanding of drug development processes, and a proven track record in clinical research. Essential skills include critical thinking, problem-solving, data interpretation, and exceptional written and verbal communication. You must be adept at using various clinical trial management software and statistical analysis tools. This role demands a high degree of autonomy, self-discipline, and the ability to manage multiple projects concurrently without direct supervision. We value individuals who are passionate about advancing healthcare and are committed to scientific rigor and ethical research practices. Your contributions will directly impact patient outcomes and the future pipeline of our client. This remote position requires a reliable internet connection and a dedicated workspace conducive to focused work and secure virtual collaboration.
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0
Clinical Research Scientist
90100 Mangu
KES180000 Annually
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Posted 12 days ago
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Job Description
Our client, a prominent entity in the pharmaceutical sector, is looking for a dedicated and innovative Clinical Research Scientist to join their forward-thinking team. This role is essential in advancing the development of novel therapeutics and ensuring the highest standards of clinical research. The position offers a hybrid work model, providing flexibility while maintaining essential in-person collaboration. Your primary responsibilities will include designing, planning, and executing clinical trials, analyzing complex trial data, and interpreting results to guide further research and development efforts. You will be involved in all phases of the clinical trial lifecycle, from protocol development and investigator selection to data monitoring and final study reports. A critical part of your role will be to ensure that all research activities comply with regulatory guidelines (e.g., GCP, FDA, EMA) and ethical standards. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and R&D, as well as external investigators and key opinion leaders. The ideal candidate will possess strong scientific acumen, excellent analytical and statistical skills, and a deep understanding of pharmaceutical drug development processes. Experience in a specific therapeutic area may be advantageous. This role requires exceptional organizational skills, the ability to manage multiple projects concurrently, and a meticulous attention to detail. You will contribute to the scientific literature through publications and presentations. We are seeking a candidate who is passionate about scientific discovery and committed to improving patient outcomes through rigorous clinical research. The position requires strong communication abilities and a proactive approach to problem-solving within the Machakos, Machakos, KE area, with a hybrid work arrangement.
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Clinical Research Scientist - Oncology
00100 Abothuguchi West
KES250000 Annually
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Posted today
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Our client, a leading global biopharmaceutical company dedicated to developing innovative therapies for unmet medical needs, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology. This is a fully remote position, offering the flexibility to contribute to groundbreaking research from anywhere. You will be instrumental in designing, developing, and executing clinical trial protocols for novel cancer treatments. Your role will involve collaborating closely with cross-functional teams, including medical affairs, regulatory affairs, data management, and external investigators, to ensure the successful progression of clinical studies. Key responsibilities include literature reviews, developing study concepts and protocols, preparing regulatory submission documents, and providing scientific expertise throughout the clinical development process. You will also analyze clinical data, interpret study results, and contribute to scientific publications and presentations. This position requires a deep understanding of oncology, clinical trial methodologies, and regulatory guidelines (e.g., ICH-GCP). You will be expected to stay abreast of the latest scientific advancements in cancer research and drug development. The ideal candidate possesses strong analytical, critical thinking, and problem-solving skills, with a proven ability to manage complex projects independently. Excellent communication and interpersonal skills are essential for effective collaboration with internal teams and external partners. Qualifications include a Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Molecular Biology, Pharmacology). A minimum of 5 years of experience in clinical research, preferably within the pharmaceutical industry and with a focus on oncology, is required. Demonstrated experience in protocol development, study design, and clinical data analysis is essential. Familiarity with various therapeutic areas within oncology is highly advantageous. This remote opportunity provides an exciting chance to contribute to the advancement of cancer therapies and work within a highly collaborative and scientifically driven organization. Join us to make a real difference in the lives of patients.
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2
Senior Clinical Research Scientist
80200 Shella
KES220000 Annually
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Posted today
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Job Description
Our client, a leading innovator in the pharmaceutical industry, is seeking a highly experienced Senior Clinical Research Scientist to join their cutting-edge, remote-first research and development team. This role is critical for advancing our client's pipeline of novel therapeutics. You will be responsible for the design, execution, and interpretation of clinical trials, playing a key role in bringing life-saving medications to market. The ideal candidate possesses a strong scientific background, extensive experience in clinical trial methodology, and a deep understanding of regulatory requirements. As a fully remote employee, you will collaborate virtually with cross-functional teams, including R&D, regulatory affairs, biostatistics, and clinical operations. Your expertise will be essential in developing robust clinical development strategies, authoring study protocols, and ensuring the highest standards of scientific rigor and data integrity. This position demands a proactive approach, excellent analytical skills, and the ability to lead and influence scientific discussions. Key responsibilities include: Designing and developing innovative clinical trial protocols that align with scientific objectives and regulatory guidelines. Overseeing the execution of clinical trials, ensuring adherence to protocols, GCP, and regulatory standards. Analyzing and interpreting clinical trial data, generating key insights, and preparing comprehensive study reports. Authoring scientific publications, regulatory submissions, and internal research documents. Collaborating with internal and external stakeholders, including investigators, key opinion leaders (KOLs), and regulatory agencies. Contributing to the development of clinical pharmacology strategies and dose selection for new drug candidates. Evaluating and integrating emerging scientific literature and methodologies into clinical development plans. Providing scientific guidance and mentorship to junior research staff. Staying abreast of advancements in relevant therapeutic areas and clinical research methodologies. Ensuring the scientific validity and ethical conduct of all clinical research activities. Qualifications: Ph.D. or M.D. in a relevant scientific discipline (e.g., Pharmacology, Toxicology, Medicine, Biology). Minimum of 7 years of experience in clinical research within the pharmaceutical or biotechnology industry. Proven experience in designing, conducting, and analyzing Phase I-III clinical trials. Strong understanding of drug development processes, regulatory affairs (FDA, EMA), and GCP guidelines. Excellent scientific writing skills, with a track record of publications and presentations. Demonstrated ability to critically evaluate scientific data and make sound scientific judgments. Strong leadership, collaboration, and communication skills. Experience in the specified therapeutic area is highly desirable. Ability to work independently and manage multiple complex projects in a remote environment. This is a fully remote position, supporting the scientific direction and clinical trial oversight for projects impacting the **Malindi, Kilifi, KE** region, though the role operates globally from a remote standpoint.
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3
Clinical Research Scientist - Remote
00100 Abothuguchi West
KES380000 Annually
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Posted today
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Job Description
Our client is a leading pharmaceutical research organization seeking a highly qualified and dedicated Clinical Research Scientist to join their innovative team on a fully remote basis. This role is critical in advancing drug development pipelines and ensuring the efficacy and safety of new pharmaceutical products. You will be responsible for designing, implementing, and managing clinical trials, from protocol development to data analysis and reporting. This includes selecting appropriate research methodologies, identifying and recruiting trial sites and investigators, and ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. Your expertise in clinical pharmacology, biostatistics, and data management will be essential. You will collaborate closely with internal R&D teams, external collaborators, and regulatory agencies (like the Pharmacy and Poisons Board) to ensure the successful execution of clinical studies. The ability to interpret complex scientific data, identify trends, and make informed recommendations for study design and analysis is paramount. This position requires a meticulous and results-driven individual with a strong scientific background and a passion for improving patient health. This is an exceptional opportunity for a seasoned scientist to contribute to groundbreaking pharmaceutical research from the convenience of a remote work environment. You will be instrumental in bringing life-changing therapies to market. We are looking for a strategic thinker with excellent problem-solving skills and a deep understanding of the pharmaceutical industry. Your contribution will be vital in ensuring the integrity and success of our clinical research programs. If you are driven by scientific curiosity and possess a commitment to excellence in clinical research, we invite you to apply for this challenging and rewarding remote role.
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4
Clinical Research Scientist - Oncology
01001 Ngong
KES4200000 Annually
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Posted today
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Our client, a pioneering pharmaceutical company dedicated to advancing cancer treatments, is seeking a highly skilled Clinical Research Scientist specializing in Oncology. This is a fully remote position, offering the chance to contribute to life-saving research from anywhere. You will be instrumental in the design, execution, and analysis of clinical trials for novel oncology therapeutics. Your responsibilities will include developing study protocols, writing investigator brochures, and overseeing data collection and interpretation. You will collaborate closely with principal investigators, regulatory bodies, and internal teams to ensure compliance with all relevant guidelines and ethical standards. The ideal candidate will possess a Ph.D. or M.D. in a relevant scientific discipline, with a strong background in oncology and clinical trial methodology. Proven experience in designing and managing Phase I-III clinical trials is essential. You must have a comprehensive understanding of oncology drug development, pharmacokinetics, pharmacodynamics, and statistical analysis principles. Excellent written and verbal communication skills are critical for preparing scientific documents, publishing research findings, and presenting complex data to diverse audiences. The ability to work independently, manage multiple projects concurrently, and thrive in a remote, collaborative environment is paramount. You will be expected to stay abreast of the latest advancements in cancer research and clinical practice. This role offers a unique opportunity to make a profound impact on patient outcomes and drive innovation in pharmaceutical research, supporting critical trials associated with medical advancements near **Ruiru, Kiambu, KE**, and beyond, all within a remote work framework.
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5
Senior Clinical Research Scientist
01001 Ngong
KES200000 Annually
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Posted today
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Job Description
Our client, a leading pharmaceutical innovator, is seeking an exceptional Senior Clinical Research Scientist to join their fully remote global research team. This vital role will involve designing, implementing, and managing complex clinical trials that contribute to the development of groundbreaking new therapies. You will be responsible for interpreting complex scientific data, ensuring the scientific integrity of trials, and collaborating with cross-functional teams including clinical operations, regulatory affairs, and data management. The ideal candidate will possess a deep understanding of drug development processes, strong analytical skills, and a passion for advancing medical science. This is a unique opportunity to contribute to life-saving research from a remote setting.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design and develop clinical trial protocols in accordance with regulatory guidelines and scientific objectives.
- Oversee the execution of clinical trials, ensuring adherence to protocols and quality standards.
- Analyze and interpret complex clinical trial data, preparing comprehensive reports.
- Collaborate with internal and external stakeholders, including investigators, study coordinators, and regulatory agencies.
- Contribute to the preparation of regulatory submission documents (e.g., IND, NDA).
- Identify and evaluate potential new drug candidates and therapeutic strategies.
- Stay current with scientific literature, clinical trial methodologies, and regulatory requirements.
- Mentor junior research scientists and provide scientific guidance.
- Manage research budgets and timelines effectively.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., pharmacology, toxicology, biochemistry, medicine).
- Minimum of 7 years of experience in clinical research, drug development, or a related field within the pharmaceutical or biotechnology industry.
- Proven expertise in clinical trial design, execution, and data analysis.
- In-depth knowledge of ICH-GCP guidelines and other relevant regulatory requirements.
- Exceptional scientific writing and communication skills.
- Strong analytical and critical thinking abilities.
- Demonstrated ability to work effectively in a remote, cross-functional team environment.
- Experience with statistical analysis software and data management systems is a plus.
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6
Senior Clinical Research Scientist
60100 Embu, Eastern
KES150000 Annually
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Posted 2 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking an accomplished Senior Clinical Research Scientist to contribute to groundbreaking drug development efforts. This position involves a hybrid work model, offering a blend of remote flexibility and in-office collaboration at our state-of-the-art facilities. You will play a crucial role in the design, execution, and analysis of clinical trials, ensuring compliance with regulatory standards and contributing to the advancement of novel therapeutics. This role requires a rigorous scientific background, exceptional analytical skills, and a deep understanding of clinical research methodologies.
Key Responsibilities:
Qualifications:
This is a critical role within our client's research and development division. The successful candidate will have the opportunity to shape the future of pharmaceutical innovation. If you are a dedicated and experienced clinical research professional seeking a challenging role with a focus on scientific excellence, we encourage you to apply. The hybrid nature of this role requires a presence in Embu, Embu, KE , balanced with remote work flexibility.
Key Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific validity and regulatory compliance.
- Oversee the conduct of clinical trials, monitoring progress, and ensuring data integrity.
- Analyze clinical trial data, interpret results, and contribute to scientific publications and regulatory submissions.
- Collaborate with cross-functional teams, including regulatory affairs, medical affairs, and biostatistics.
- Manage relationships with investigators, study sites, and contract research organizations (CROs).
- Ensure adherence to Good Clinical Practice (GCP) guidelines and other relevant regulations.
- Contribute to the strategic planning of clinical development programs.
- Prepare clinical study reports and summaries for internal and external stakeholders.
- Stay abreast of the latest scientific advancements and therapeutic areas relevant to the company's pipeline.
- Mentor junior members of the clinical research team.
Qualifications:
- Ph.D. or M.D. in a relevant scientific discipline (e.g., pharmacology, biology, medicine).
- Minimum of 7 years of experience in clinical research, with a strong focus on drug development in the pharmaceutical industry.
- Demonstrated experience in designing and executing clinical trials across various phases.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Excellent data analysis and interpretation skills.
- Strong scientific writing and communication abilities.
- Proven ability to collaborate effectively in a multidisciplinary team environment.
- Experience managing CROs and external vendors.
- Strategic thinking and problem-solving capabilities.
- Ability to balance remote work with required on-site responsibilities.
This is a critical role within our client's research and development division. The successful candidate will have the opportunity to shape the future of pharmaceutical innovation. If you are a dedicated and experienced clinical research professional seeking a challenging role with a focus on scientific excellence, we encourage you to apply. The hybrid nature of this role requires a presence in Embu, Embu, KE , balanced with remote work flexibility.
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7
Clinical Research Scientist (Remote)
01001 Ngong
KES180000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading innovator in the pharmaceutical industry, is searching for a dedicated and experienced Clinical Research Scientist to join their global, remote-first research team. This role is crucial for the design, execution, and analysis of clinical trials that drive the development of life-saving therapies. You will be responsible for contributing to the scientific strategy of clinical development programs, ensuring the highest standards of research integrity and regulatory compliance. The ideal candidate will possess a strong scientific background, extensive knowledge of clinical trial methodologies, and a proven track record in drug development. You must be adept at analyzing complex data, interpreting results, and translating scientific findings into actionable insights. Collaboration will be key, as you will work closely with internal teams, external investigators, and regulatory bodies. This position demands meticulous attention to detail, excellent problem-solving skills, and the ability to manage multiple projects simultaneously. As a fully remote role, you will need exceptional self-discipline and communication skills to thrive. Responsibilities include: Designing clinical trial protocols, investigator brochures, and other study documents. Contributing to the scientific and strategic direction of clinical development plans. Overseeing the execution of clinical trials, ensuring adherence to protocols and Good Clinical Practice (GCP) guidelines. Analyzing and interpreting clinical data, identifying trends and potential safety issues. Preparing scientific reports, publications, and presentations for internal and external stakeholders. Collaborating with biostatistics and data management teams to ensure data quality and integrity. Providing scientific guidance to clinical operations and regulatory affairs teams. Staying abreast of the latest scientific advancements, therapeutic areas, and competitive landscape. Contributing to the preparation of regulatory submissions (e.g., IND, NDA). Managing relationships with key opinion leaders and clinical investigators. Qualifications: PhD or equivalent in a relevant scientific discipline (e.g., Pharmacology, Biology, Medicine). Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry. Deep understanding of drug development process and regulatory requirements (FDA, EMA). Strong analytical and statistical skills, with experience in data interpretation. Excellent written and verbal communication skills, with a strong publication record. Proven ability to design and manage clinical trials. Experience with various therapeutic areas is a plus. Ability to work independently and effectively within a remote, global team environment. Strong project management and organizational skills. This is an exciting opportunity to contribute to groundbreaking medical advancements and shape the future of patient care through innovative pharmaceutical solutions, all from the convenience of your home office.
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8
Clinical Research Scientist - Oncology
00200 Ongata Rongai, Rift Valley
KES220000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client is seeking a dedicated and highly qualified Clinical Research Scientist specializing in Oncology to join their pioneering remote research team. This crucial role involves the design, execution, and interpretation of clinical trials aimed at advancing cancer therapies. You will be responsible for overseeing all aspects of clinical research studies, including protocol development, site selection and management, data analysis, and regulatory submissions. The ideal candidate will possess a strong scientific background, a deep understanding of oncology drug development, and extensive experience in clinical trial design and management. You will collaborate with internal and external stakeholders, including investigators, study coordinators, and regulatory agencies, ensuring adherence to Good Clinical Practice (GCP) guidelines and all applicable regulations. A key focus will be on leveraging cutting-edge research methodologies and data to drive scientific innovation. This is a remote-first position, allowing you to contribute your expertise from **Ongata Rongai, Kajiado, KE**, or any other location globally. We seek a meticulous researcher with excellent analytical, problem-solving, and communication skills, capable of leading complex projects in a virtual environment and contributing to life-saving advancements in cancer treatment.
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