99 Oncology jobs in Kenya
Clinical Research Scientist - Oncology
20201 Kapsuser
KES2200000 Annually
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Posted 3 days ago
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Job Description
Our client, a pioneering pharmaceutical company at the forefront of cancer research, is seeking a highly specialized and driven Clinical Research Scientist – Oncology to join our innovative, fully remote R&D team. This position offers a unique chance to contribute to groundbreaking advancements in cancer therapeutics and patient care, all while working from a remote location. You will play a critical role in the design, execution, and analysis of clinical trials, driving the development of life-saving medications.
Key Responsibilities:
Key Responsibilities:
- Design and develop clinical trial protocols for novel oncology drugs, ensuring scientific rigor and regulatory compliance.
- Oversee the conduct of clinical trials, including patient recruitment, data collection, and monitoring of safety and efficacy.
- Analyze clinical trial data, interpret results, and prepare comprehensive reports for regulatory submissions and scientific publications.
- Collaborate closely with cross-functional teams, including R&D, medical affairs, regulatory affairs, and external investigators, in a virtual environment.
- Manage relationships with Key Opinion Leaders (KOLs) and investigators, providing scientific expertise and support.
- Stay abreast of the latest scientific literature, emerging therapeutic targets, and advancements in oncology drug development.
- Contribute to the development of scientific strategy and identify new research opportunities.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
- Prepare and present scientific findings at internal meetings and external conferences.
- Provide scientific input for regulatory filings and responses to health authority queries.
- Contribute to the training and mentoring of junior research staff remotely.
- PhD or MD in a relevant scientific discipline (e.g., Oncology, Pharmacology, Molecular Biology, Biochemistry).
- Minimum of 5 years of experience in clinical research, specifically within the oncology therapeutic area.
- In-depth knowledge of cancer biology, drug development processes, and clinical trial methodologies.
- Proven experience in designing, managing, and analyzing oncology clinical trials.
- Strong understanding of regulatory requirements (e.g., FDA, EMA) and GCP guidelines.
- Excellent analytical, statistical, and problem-solving skills.
- Exceptional written and verbal communication skills, with the ability to articulate complex scientific concepts.
- Demonstrated ability to work independently and collaboratively in a remote, fast-paced environment.
- Strong project management skills and ability to manage multiple priorities.
- Experience with data analysis software and statistical packages is a plus.
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0
Clinical Research Scientist - Oncology
20400 Naivasha, Rift Valley
KES180000 Annually
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Posted 4 days ago
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Job Description
Our client is seeking an accomplished Clinical Research Scientist specializing in Oncology to join their groundbreaking research division. This is a fully remote position, allowing you to contribute to cutting-edge pharmaceutical research from any location. The primary focus of this role will be to design, implement, and analyze clinical trials that evaluate the efficacy and safety of novel cancer therapies. You will play a crucial part in the drug development lifecycle, from preclinical stages through to post-market surveillance. Responsibilities include developing study protocols, creating clinical trial documentation, managing investigator sites, ensuring regulatory compliance, and interpreting complex scientific data. The ideal candidate will possess a strong scientific background, excellent analytical and problem-solving skills, and a thorough understanding of clinical trial methodologies and pharmaceutical regulations. You will collaborate closely with cross-functional teams, including biostatisticians, medical monitors, and regulatory affairs specialists. A deep understanding of oncology, including various cancer types, treatment modalities, and current research trends, is essential. We are looking for an individual who is detail-oriented, meticulous, and committed to advancing cancer treatment through rigorous scientific inquiry. This remote role demands excellent written and verbal communication skills, as you will be presenting findings to internal stakeholders and potentially external scientific communities. A Ph.D. or Master's degree in a relevant life science field (e.g., Biology, Pharmacology, Medicine) is required, along with a minimum of 5 years of experience in clinical research, preferably within the oncology therapeutic area. Experience with GCP (Good Clinical Practice) guidelines and regulatory submissions (e.g., FDA, EMA) is mandatory. The ability to work independently, manage multiple projects simultaneously, and meet strict deadlines in a remote setting is crucial. This is a unique opportunity to contribute significantly to life-saving medical advancements while enjoying the benefits of a flexible, remote work arrangement. If you are driven by scientific excellence and passionate about making a difference in the lives of cancer patients, we invite you to apply.
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1
Clinical Research Scientist - Oncology
80100 Nairobi, Nairobi
KES900000 Annually
WhatJobs
Posted 11 days ago
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Job Description
Our client, a global pharmaceutical innovator dedicated to advancing healthcare, is seeking a highly motivated Clinical Research Scientist specializing in Oncology. This is a crucial fully remote role where you will contribute to the development of life-saving cancer treatments. You will be responsible for the design, execution, and analysis of clinical trials, ensuring adherence to rigorous scientific and regulatory standards. The ideal candidate possesses a Ph.D. or M.D. in a relevant life science discipline, with a strong background in oncology research and clinical trial methodology. Your expertise will be vital in interpreting complex data, developing study protocols, and collaborating with investigators, regulatory bodies, and internal teams to bring novel therapies to patients. This remote position allows you to make a significant impact from anywhere, contributing to advancements for patients in the **Mombasa, Mombasa, KE** region and worldwide. Responsibilities include reviewing scientific literature, preparing regulatory submissions, and contributing to the scientific strategy of drug development programs. You will also play a key role in data analysis and interpretation, manuscript preparation, and scientific presentations. Exceptional analytical, communication, and project management skills are essential. Experience with biostatistics, pharmacokinetics, and pharmacodynamics is highly desirable. Join us in our mission to transform patient care through cutting-edge pharmaceutical research.
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2
Clinical Research Scientist - Oncology
70100 Abothuguchi West
KES180000 Annually
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Posted 12 days ago
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Job Description
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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3
Clinical Research Scientist - Oncology
N/A Meru , Eastern
KES420000 Annually
WhatJobs
Posted 14 days ago
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Job Description
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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4
Clinical Research Scientist - Oncology
20101 Mwembe
KES250000 Annually
WhatJobs
Posted 14 days ago
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Job Description
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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5
Clinical Research Associate - Oncology
20100 Mwembe
KES250000 Annually
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Posted 14 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their growing team in Nakuru, Nakuru, KE . This role is crucial for the successful execution of clinical trials, particularly within the field of oncology, ensuring data integrity, patient safety, and adherence to regulatory standards. As a CRA, you will be responsible for site selection, initiation, monitoring, and close-out of clinical trial sites. This hybrid role requires a blend of remote work and on-site visits to study centers, providing flexibility while maintaining essential in-person oversight. You will serve as the primary point of contact between the sponsor and the investigative sites, fostering strong relationships and facilitating smooth trial operations. Your responsibilities will include reviewing and verifying source documents against case report forms (CRFs), ensuring compliance with Good Clinical Practice (GCP) guidelines and protocol requirements, and identifying and resolving site issues promptly. You will also be involved in training site personnel on study procedures and regulatory requirements. The ideal candidate will possess strong knowledge of clinical trial phases, drug development processes, and relevant regulatory frameworks such as FDA and EMA guidelines. Exceptional organizational skills, meticulous attention to detail, and the ability to manage multiple priorities effectively are paramount. This position demands excellent interpersonal and communication skills, enabling you to build rapport with investigators, study coordinators, and other stakeholders. You will contribute to the critical mission of bringing life-saving therapies to patients by ensuring the highest quality data and ethical conduct throughout the trial lifecycle. This is an exciting opportunity to contribute to cutting-edge research and make a tangible difference in patient care.
Responsibilities:
Responsibilities:
- Perform site qualification, initiation, interim, and close-out visits.
- Monitor clinical trial conduct according to protocol, GCP, and regulatory requirements.
- Verify accuracy, completeness, and consistency of data entered into the CRF and source documents.
- Ensure patient safety and adherence to protocol requirements.
- Train and educate site staff on study-specific procedures and regulatory compliance.
- Act as the primary liaison between the sponsor and investigative sites.
- Identify, document, and resolve site-related issues and deviations.
- Prepare and submit monitoring visit reports in a timely manner.
- Review and track essential regulatory documents.
- Participate in investigator meetings and relevant training sessions.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and applicable regulatory requirements.
- Experience in oncology clinical trials is highly preferred.
- Strong understanding of medical terminology and clinical trial procedures.
- Excellent communication, interpersonal, and organizational skills.
- Ability to travel to investigative sites as required.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Strong problem-solving abilities and attention to detail.
- Ability to work independently and as part of a team.
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6
Clinical Research Scientist - Oncology
00100 Abothuguchi West
KES250000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
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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7
Clinical Research Scientist - Oncology
01001 Ngong
KES4200000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
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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8
Clinical Research Scientist - Oncology
00200 Ongata Rongai, Rift Valley
KES220000 Annually
WhatJobs
Posted 14 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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