5,058 Oncology Research jobs in Kenya
Clinical Research Scientist - Oncology
70100 Abothuguchi West
KES180000 Annually
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Our client, a leading global biopharmaceutical company dedicated to advancing cancer therapies, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology. This position is a critical part of our client's remote-first research and development division, focused on driving groundbreaking clinical trials from inception through to regulatory submission. You will be instrumental in designing clinical trial protocols, analyzing complex datasets, and interpreting results to advance the development of novel oncology treatments. The ideal candidate will possess a deep scientific understanding of cancer biology, extensive experience in clinical trial management, and a strong publication record. As a fully remote role, you will collaborate extensively with a global team of scientists, clinicians, and statisticians, leveraging cutting-edge digital collaboration platforms. Key responsibilities include:
- Designing and developing innovative clinical trial protocols for oncology therapeutics, ensuring alignment with scientific objectives and regulatory requirements.
- Overseeing the execution of clinical trials, from site selection and initiation to data collection and analysis.
- Analyzing and interpreting complex clinical trial data, including safety and efficacy endpoints.
- Collaborating with biostatisticians to develop statistical analysis plans and interpret results.
- Authoring clinical study reports, regulatory submission documents (e.g., IND, NDA), and scientific publications.
- Providing scientific and clinical expertise to internal teams and external investigators.
- Staying abreast of the latest advancements in oncology research, drug development, and regulatory landscapes.
- Evaluating new technologies and methodologies for clinical research.
- Managing relationships with key opinion leaders (KOLs) and clinical investigators.
- Contributing to the strategic direction of the oncology pipeline.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Molecular Biology, Pharmacology, Oncology, Immunology).
- Minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a specific focus on oncology.
- Proven experience in designing and managing Phase I-III clinical trials.
- Strong understanding of cancer biology, immunology, and therapeutic targets.
- Demonstrated expertise in data analysis, interpretation, and scientific writing.
- Familiarity with regulatory guidelines (FDA, EMA) for drug development.
- Excellent communication, presentation, and collaboration skills.
- Ability to work effectively in a remote, cross-functional team environment.
- Strong project management and problem-solving abilities.
- This key scientific position is conceptually located in Garissa, Garissa, KE , however, it is a fully remote role.
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0
Clinical Research Scientist - Oncology
N/A Meru , Eastern
KES420000 Annually
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Posted 2 days ago
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Our client, a pioneering pharmaceutical company dedicated to advancing cancer therapies, is looking for a highly motivated and experienced Clinical Research Scientist specializing in Oncology. This position is entirely remote, offering flexibility and the chance to contribute to life-saving research from anywhere. You will play a critical role in the design, execution, and analysis of clinical trials for novel oncology drugs. Responsibilities include developing study protocols, selecting and managing clinical sites, overseeing data collection and integrity, and interpreting complex clinical data. The ideal candidate will possess a deep understanding of oncology, clinical trial methodologies, and regulatory requirements (e.g., FDA, EMA). You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and data management, to ensure the successful and timely completion of clinical studies. Strong analytical and problem-solving skills, coupled with excellent written and verbal communication abilities, are essential. This role offers an exceptional opportunity to make a significant impact on patient outcomes and advance your career in a rapidly evolving field. You will be at the forefront of drug development, working with cutting-edge treatments and contributing to the global fight against cancer. We value scientific rigor, ethical conduct, and a collaborative spirit. Join our client's mission to bring hope and healing to patients worldwide. The successful candidate will demonstrate a passion for scientific discovery and a commitment to delivering high-quality research.
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Clinical Research Scientist - Oncology
20101 Mwembe
KES250000 Annually
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Posted 2 days ago
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Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Clinical Research Scientist specializing in Oncology. This is a critical role focused on the design, execution, and interpretation of clinical trials aimed at developing novel cancer therapies. You will be instrumental in bringing life-changing treatments to patients by contributing to all phases of clinical development, from early-stage research to post-market surveillance. The ideal candidate possesses a strong scientific background, a deep understanding of oncology, and a proven ability to manage complex clinical research projects. Responsibilities include developing clinical trial protocols, overseeing data collection and analysis, and collaborating closely with investigators, study sites, and regulatory agencies. You will be responsible for ensuring adherence to Good Clinical Practice (GCP) guidelines and all relevant regulatory requirements. This role demands excellent analytical skills, critical thinking, and the ability to communicate complex scientific information effectively to diverse audiences, including internal teams, external investigators, and regulatory bodies. The candidate will actively contribute to the scientific strategy for oncology drug development, identifying new research opportunities and shaping the direction of future studies. This position offers a hybrid work arrangement, providing the flexibility to work remotely while also engaging in essential on-site activities for collaboration and study oversight. You will play a vital part in advancing our understanding of cancer and developing innovative therapeutic solutions. Responsibilities:
- Design, develop, and execute clinical trial protocols for oncology assets.
- Oversee the planning and conduct of clinical trials, ensuring compliance with GCP and regulatory standards.
- Analyze and interpret clinical trial data, contributing to study reports and regulatory submissions.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, R&D, and commercial departments.
- Serve as a key scientific expert for assigned oncology projects.
- Provide scientific guidance and support to clinical study sites and investigators.
- Prepare scientific publications, presentations, and regulatory documentation.
- Monitor the competitive landscape and emerging scientific advancements in oncology.
- Contribute to the strategic direction of the oncology pipeline.
- Evaluate and implement new methodologies and technologies in clinical research.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Biology, Pharmacology, Medicine).
- Minimum of 5 years of experience in clinical research within the pharmaceutical industry, with a strong focus on oncology.
- Demonstrated expertise in clinical trial design, execution, and data analysis.
- In-depth knowledge of oncology, including disease pathophysiology, treatment paradigms, and drug development.
- Familiarity with GCP, ICH guidelines, and global regulatory requirements.
- Excellent scientific writing and communication skills.
- Strong analytical and problem-solving abilities.
- Ability to work effectively in a hybrid work environment, balancing remote and on-site responsibilities.
- Experience with oncology clinical endpoints and biomarkers.
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Clinical Research Scientist - Oncology
00100 Abothuguchi West
KES250000 Annually
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Posted 2 days ago
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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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3
Clinical Research Scientist - Oncology
01001 Ngong
KES4200000 Annually
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Posted 2 days ago
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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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4
Clinical Research Scientist - Oncology
00200 Ongata Rongai, Rift Valley
KES220000 Annually
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Posted 2 days ago
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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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5
Clinical Research Scientist - Oncology
40100 Tuwan
KES220000 Annually
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Posted 2 days ago
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Our client, a pioneering pharmaceutical company at the forefront of medical innovation, is actively seeking a highly skilled and dedicated Clinical Research Scientist specializing in Oncology. This is a fully remote position, offering you the flexibility to contribute to groundbreaking research from the comfort of your home office. We are committed to advancing healthcare through rigorous scientific investigation and are looking for passionate individuals to join our collaborative global team.
In this critical role, you will be instrumental in designing, implementing, and managing clinical trials for novel oncology therapeutics. Your responsibilities will encompass protocol development, site selection and initiation, data analysis, and interpretation of results. You will work closely with cross-functional teams, including medical affairs, regulatory affairs, and biostatistics, to ensure the successful execution of clinical development programs. A deep understanding of oncology, clinical trial methodologies, and regulatory guidelines (e.g., ICH-GCP) is paramount.
The ideal candidate will possess a Ph.D. or M.D. in a relevant life science discipline, with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a specific focus on oncology. Demonstrated experience in leading and contributing to Phase I-III clinical trials is essential. You should have a strong publication record in peer-reviewed journals and excellent written and verbal communication skills. The ability to analyze complex datasets, draw meaningful conclusions, and present findings clearly and concisely is a must.
Key Responsibilities:
This is an exceptional opportunity for an experienced and driven Clinical Research Scientist to contribute to the development of life-changing treatments in a fully remote, cutting-edge environment. If you are passionate about advancing cancer care through innovative research, we invite you to explore this exciting role.
In this critical role, you will be instrumental in designing, implementing, and managing clinical trials for novel oncology therapeutics. Your responsibilities will encompass protocol development, site selection and initiation, data analysis, and interpretation of results. You will work closely with cross-functional teams, including medical affairs, regulatory affairs, and biostatistics, to ensure the successful execution of clinical development programs. A deep understanding of oncology, clinical trial methodologies, and regulatory guidelines (e.g., ICH-GCP) is paramount.
The ideal candidate will possess a Ph.D. or M.D. in a relevant life science discipline, with a minimum of 5 years of experience in clinical research within the pharmaceutical or biotechnology industry, with a specific focus on oncology. Demonstrated experience in leading and contributing to Phase I-III clinical trials is essential. You should have a strong publication record in peer-reviewed journals and excellent written and verbal communication skills. The ability to analyze complex datasets, draw meaningful conclusions, and present findings clearly and concisely is a must.
Key Responsibilities:
- Design and oversee the execution of clinical studies in oncology.
- Develop clinical trial protocols, investigator brochures, and study reports.
- Monitor trial progress, ensuring adherence to protocol and regulatory requirements.
- Collaborate with internal and external stakeholders, including investigators, study coordinators, and regulatory bodies.
- Analyze and interpret clinical trial data, contributing to scientific publications and regulatory submissions.
- Provide scientific and clinical expertise on oncology drug development.
This is an exceptional opportunity for an experienced and driven Clinical Research Scientist to contribute to the development of life-changing treatments in a fully remote, cutting-edge environment. If you are passionate about advancing cancer care through innovative research, we invite you to explore this exciting role.
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6
Clinical Research Scientist - Oncology
00200 Ongata Rongai, Rift Valley
KES1500000 Annually
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Posted 2 days ago
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Job Description
Our client, a leading global pharmaceutical company, is expanding its research and development division and is seeking a highly skilled and experienced Clinical Research Scientist specializing in Oncology to join their dynamic, fully remote team. This critical role will involve designing, implementing, and monitoring clinical trials, contributing to the advancement of novel cancer therapies. The successful candidate will possess a deep understanding of oncology drug development, clinical trial methodologies, and regulatory requirements. You will play a key role in analyzing trial data, interpreting results, and contributing to scientific publications and regulatory submissions.
Key Responsibilities:
This is a fully remote position, allowing you to work from your preferred location within **Ongata Rongai, Kajiado, KE**, or other approved remote locations. We are committed to fostering a flexible and results-oriented work environment. We seek candidates who are self-motivated, possess excellent problem-solving abilities, and can work independently while maintaining strong communication with global teams. Strong written and verbal communication skills are paramount for this role, enabling effective collaboration across diverse functional areas and geographical regions. The ability to manage multiple projects simultaneously and adapt to evolving research priorities is crucial. This is an excellent opportunity for a dedicated scientist to contribute to life-saving treatments and advance their career in a cutting-edge pharmaceutical organization. The remuneration package is highly competitive and reflects the importance of this role.
Key Responsibilities:
- Design and develop clinical trial protocols in accordance with scientific and regulatory standards.
- Oversee the operational aspects of clinical trials, ensuring adherence to protocol and Good Clinical Practice (GCP).
- Collaborate with investigators, site staff, and internal teams to ensure successful trial execution.
- Analyze and interpret clinical trial data, including statistical analysis and safety assessments.
- Prepare clinical study reports (CSRs) and contribute to regulatory submissions (e.g., IND, NDA).
- Stay abreast of the latest scientific advancements and competitive landscape in oncology.
- Manage relationships with external partners, including Contract Research Organizations (CROs) and key opinion leaders (KOLs).
- Contribute to the strategic planning of drug development programs.
- Ensure compliance with all ethical and regulatory guidelines throughout the trial lifecycle.
- Mentor junior members of the clinical research team.
This is a fully remote position, allowing you to work from your preferred location within **Ongata Rongai, Kajiado, KE**, or other approved remote locations. We are committed to fostering a flexible and results-oriented work environment. We seek candidates who are self-motivated, possess excellent problem-solving abilities, and can work independently while maintaining strong communication with global teams. Strong written and verbal communication skills are paramount for this role, enabling effective collaboration across diverse functional areas and geographical regions. The ability to manage multiple projects simultaneously and adapt to evolving research priorities is crucial. This is an excellent opportunity for a dedicated scientist to contribute to life-saving treatments and advance their career in a cutting-edge pharmaceutical organization. The remuneration package is highly competitive and reflects the importance of this role.
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7
Clinical Research Scientist - Oncology
20100 Mwembe
KES150000 Annually
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Posted 2 days ago
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Job Description
Our client, a pioneering pharmaceutical research firm, is looking for a dedicated and highly qualified Clinical Research Scientist specializing in Oncology to contribute to groundbreaking therapeutic development. This hybrid role offers a blend of remote work flexibility and essential on-site collaboration. You will play a critical role in designing, implementing, and managing clinical trials for novel cancer treatments. Responsibilities include protocol development, data analysis and interpretation, scientific writing, and regulatory submissions. You will collaborate closely with cross-functional teams, including medical affairs, regulatory affairs, and data management, to ensure the successful execution of clinical studies. The ideal candidate will possess a PhD or MD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Biochemistry) and a minimum of 5 years of experience in clinical research within the pharmaceutical industry. A deep understanding of oncology drug development, clinical trial methodologies, and regulatory guidelines (e.g., ICH-GCP) is essential. You should have a proven track record in analyzing complex clinical data, publishing scientific findings, and contributing to the progression of drug candidates through the development pipeline. Excellent written and verbal communication skills are required, as is the ability to present complex scientific information clearly and concisely. This role involves both independent remote work and collaborative sessions at our client's facilities. Strong project management skills and the ability to work effectively in a team-oriented, fast-paced environment are crucial. You will be expected to stay abreast of the latest scientific advancements in oncology and contribute to the strategic direction of our research programs. Experience with statistical analysis software and electronic data capture (EDC) systems is beneficial. This position is based in **Nakuru, Nakuru, KE**, with a hybrid work arrangement.
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8
Senior Clinical Research Scientist - Oncology
20111 Mwembe
KES220000 Monthly
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Posted 2 days ago
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Our client, a globally renowned biopharmaceutical company at the cutting edge of cancer research, is actively seeking a Senior Clinical Research Scientist specializing in Oncology to join their esteemed, fully remote research division. This pivotal role involves designing, implementing, and overseeing groundbreaking clinical trials aimed at developing novel cancer therapies. You will be a key contributor to advancing our understanding of oncological diseases and translating scientific discoveries into life-saving treatments. The ideal candidate possesses a deep scientific background, extensive experience in clinical trial management, and a passion for driving innovation in cancer care. This position offers the unique opportunity to collaborate with world-class researchers and clinicians from the comfort of your home office.
Key Responsibilities:
Key Responsibilities:
- Design and develop clinical trial protocols for investigational oncology drugs, ensuring scientific rigor and regulatory compliance.
- Oversee the execution of clinical trials, from site selection and initiation to data analysis and reporting.
- Collaborate with principal investigators, study coordinators, and clinical research associates to ensure the successful conduct of trials.
- Interpret complex clinical trial data, identify trends, and contribute to scientific publications and presentations.
- Ensure adherence to Good Clinical Practice (GCP) guidelines, regulatory requirements (FDA, EMA, etc.), and internal company policies.
- Provide scientific and clinical expertise to cross-functional teams, including R&D, regulatory affairs, and marketing.
- Evaluate potential new drug candidates and therapeutic strategies for oncology.
- Prepare regulatory submission documents and respond to queries from health authorities.
- Mentor junior scientists and contribute to the development of research best practices.
- Stay abreast of the latest advancements in oncology research, therapeutic approaches, and clinical trial methodologies.
- Ph.D. or M.D. in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology, Immunology).
- Minimum of 7 years of experience in clinical research, with a strong focus on oncology drug development.
- Demonstrated experience in designing and managing Phase I, II, and III clinical trials.
- In-depth knowledge of cancer biology, tumor microenvironment, and current cancer therapies.
- Expertise in regulatory requirements and guidelines for drug development (GCP, ICH).
- Proven ability to analyze and interpret complex clinical data.
- Excellent scientific writing and presentation skills.
- Strong leadership and project management capabilities.
- Exceptional problem-solving and critical-thinking abilities.
- Experience working effectively in a remote, collaborative research environment.
- Publications in high-impact peer-reviewed journals are highly desirable.
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