1,298 Oncology Research jobs in Kenya
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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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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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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2
Lead Clinical Research Associate - Oncology
40100 Kisumu
KES120000 Annually
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Posted 4 days ago
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Our client, a prominent global pharmaceutical company at the forefront of cancer treatment research, is seeking an experienced and dedicated Lead Clinical Research Associate (CRA) to join their dynamic, remote-first team. In this vital role, you will oversee and manage the execution of Phase I-III clinical trials within the oncology therapeutic area. Your primary responsibility will be to ensure the smooth and efficient conduct of studies, adhering to ICH-GCP guidelines, regulatory requirements, and company protocols. This position offers the unique opportunity to manage clinical operations from anywhere, contributing to life-saving advancements in cancer therapy. You will be responsible for site selection, initiation, monitoring, and close-out activities, building strong relationships with investigators and site staff. The Lead CRA will also play a key role in training and mentoring junior CRAs, ensuring high standards of data quality and patient safety. Excellent organizational skills, meticulous attention to detail, and a proactive approach to problem-solving are essential. You must be adept at navigating complex therapeutic areas like oncology, understanding the nuances of patient care and research in this field. Proficiency in clinical trial management software (CTMS), electronic data capture (EDC) systems, and electronic trial master files (eTMF) is required. The ideal candidate will have a strong understanding of regulatory submissions and auditing processes. Exceptional communication and interpersonal skills are crucial for effective collaboration with cross-functional teams, including data management, regulatory affairs, and drug safety departments. If you are passionate about advancing cancer research and are looking for a challenging and rewarding remote career opportunity, we encourage you to apply.
Responsibilities:
Responsibilities:
- Plan, manage, and coordinate clinical trial activities at investigative sites, ensuring adherence to protocols and regulatory requirements.
- Perform site visits (remote and/or in-person as needed, though this role is remote-first) for site evaluation, initiation, routine monitoring, and close-out.
- Verify accuracy and completeness of clinical data through source document verification.
- Ensure patient safety and protocol compliance throughout the trial lifecycle.
- Train and mentor site staff and junior CRAs on study procedures and regulatory guidelines.
- Manage study supplies and investigational product at clinical sites.
- Liaise with investigators, study coordinators, and other site personnel to resolve data queries and ensure timely reporting.
- Prepare and present study progress reports to project teams and management.
- Contribute to the development of study protocols, case report forms (CRFs), and other study documents.
- Ensure all site documentation is maintained in the Trial Master File (TMF).
- Bachelor's degree in a life science, nursing, or a related field; advanced degree preferred.
- Minimum of 4-6 years of direct clinical monitoring experience, with a significant portion in oncology.
- Thorough knowledge of ICH-GCP guidelines, FDA regulations, and other applicable regulatory requirements.
- Experience with EDC systems (e.g., Medidata Rave, Oracle Clinical) and CTMS.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Ability to travel domestically and internationally as needed (though the role is primarily remote).
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3
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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4
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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5
Lead Research Scientist - Oncology
80100 Nairobi, Nairobi
KES250000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical innovator, is seeking a highly accomplished Lead Research Scientist specializing in Oncology to join their cutting-edge research team based in Mombasa, Mombasa, KE . This role offers a hybrid work arrangement, allowing for a blend of in-office collaboration and remote flexibility. You will be at the forefront of discovering and developing novel cancer therapies, driving scientific innovation from early-stage research through to preclinical development. This is an exceptional opportunity to contribute to groundbreaking work that has the potential to transform patient lives.
Key Responsibilities:
Key Responsibilities:
- Design and execute complex in vitro and in vivo experiments to investigate novel therapeutic targets and agents in oncology.
- Lead a team of research associates and scientists, providing scientific direction, mentorship, and performance management.
- Analyze experimental data, interpret results, and develop innovative solutions to scientific challenges.
- Prepare high-quality scientific reports, manuscripts for publication, and presentations for internal and external audiences.
- Collaborate closely with cross-functional teams, including medicinal chemistry, pharmacology, and clinical development, to advance drug candidates.
- Manage research projects, including resource allocation, timeline management, and budget oversight.
- Stay current with the latest scientific literature, technologies, and therapeutic trends in oncology.
- Contribute to the development of intellectual property and patent filings.
- Ensure compliance with all laboratory safety regulations and ethical guidelines.
- Present research findings at scientific conferences and symposia.
- Troubleshoot experimental issues and develop alternative approaches when necessary.
- Contribute to the strategic direction of the oncology research program.
- Mentor junior scientists and foster a collaborative and productive research environment.
- Ph.D. in Cancer Biology, Molecular Biology, Pharmacology, or a related field.
- Minimum of 7 years of postdoctoral and/or industry research experience in oncology drug discovery.
- Demonstrated expertise in cancer biology, signaling pathways, and therapeutic modalities.
- Proven experience in leading and mentoring research teams.
- Strong track record of publications in high-impact peer-reviewed journals and presentations at international conferences.
- Proficiency in a wide range of molecular and cellular biology techniques, including cell culture, Western blotting, qPCR, flow cytometry, and IHC.
- Experience with preclinical in vivo models of cancer is highly desirable.
- Excellent analytical, critical thinking, and problem-solving skills.
- Exceptional written and verbal communication skills.
- Ability to thrive in a fast-paced, collaborative, and dynamic research environment.
- Proficiency in data analysis software (e.g., GraphPad Prism, R) and laboratory information management systems (LIMS).
- Commitment to scientific rigor and ethical conduct.
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6
Lead Clinical Research Scientist (Remote)
20200 Kapsuser
KES300000 Annually
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Job Description
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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7
Clinical Research Associate
40100 Kisumu
KES190000 Annually
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Posted 1 day ago
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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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Clinical Research Associate
00100 Abothuguchi West
KES120000 month
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Posted 2 days ago
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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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