6,341 Research And Development jobs in Kenya
Agronomist - Crop Research & Development
20100 Mwembe
KES150000 Monthly
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Our client is seeking a dedicated Agronomist with a strong background in crop research and development to join their growing team. This position offers a hybrid work model, combining remote flexibility with necessary on-site engagement. You will play a crucial role in developing and implementing innovative agricultural practices to enhance crop yield, quality, and sustainability. Your responsibilities will include designing and executing field trials, analyzing data, and providing expert recommendations to farmers and agricultural businesses. You will also be involved in the evaluation of new crop varieties, fertilizers, and pest management strategies. The ability to translate scientific research into practical, actionable advice for agricultural stakeholders is paramount.
Key duties include:
Key duties include:
- Planning, conducting, and monitoring agricultural experiments and field trials.
- Collecting, interpreting, and reporting on agronomic data.
- Developing best practice guidelines for crop cultivation and management.
- Assisting in the selection and breeding of improved crop varieties.
- Providing technical support and training to farming communities.
- Staying informed about the latest advancements in agronomy and sustainable agriculture.
- Collaborating with research institutions and industry partners.
- Ensuring compliance with environmental regulations and safety standards.
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0
Senior Biophysicist - Research & Development
80101 Shella
KES150000 Annually
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Posted 6 days ago
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Our client is a leading scientific research institution seeking an innovative Senior Biophysicist to join their dynamic R&D team based in Malindi, Kilifi, KE . This hybrid role offers the opportunity to contribute to groundbreaking research in a collaborative and stimulating environment. The ideal candidate will possess a strong theoretical foundation in biophysics, coupled with extensive hands-on experience in experimental design and data analysis. You will be involved in designing, conducting, and analyzing complex experiments focused on understanding biological systems at the molecular and cellular levels. This includes utilizing advanced spectroscopic techniques, microscopy, and computational modeling to investigate protein dynamics, molecular interactions, and cellular processes. A significant part of your role will involve developing novel methodologies and experimental protocols to address challenging research questions. You will be responsible for managing research projects from conception to completion, including securing funding through grant proposals and supervising junior researchers and technicians. Effective collaboration with interdisciplinary teams, including chemists, biologists, and engineers, will be essential for the success of our research endeavors. Presenting research findings at scientific conferences and publishing in peer-reviewed journals will be a key expectation. The ability to interpret complex datasets, troubleshoot experimental challenges, and maintain meticulous laboratory records is crucial. We are looking for a highly motivated individual with a passion for scientific discovery and a commitment to pushing the boundaries of biophysical research. Experience with high-throughput screening and assay development is also highly desirable.
Responsibilities:
Qualifications:
Responsibilities:
- Design, execute, and interpret complex biophysical experiments.
- Develop and validate novel experimental techniques and methodologies.
- Investigate molecular mechanisms, protein-ligand interactions, and cellular dynamics.
- Utilize advanced instrumentation such as spectroscopy, mass spectrometry, and electron microscopy.
- Apply computational modeling and data analysis techniques to biological problems.
- Manage research projects, including planning, budgeting, and resource allocation.
- Write and submit grant proposals to secure research funding.
- Supervise and mentor junior scientists, postdocs, and research technicians.
- Collaborate effectively with interdisciplinary research teams.
- Disseminate research findings through publications and conference presentations.
- Maintain comprehensive laboratory notebooks and detailed experimental records.
- Ensure compliance with all laboratory safety regulations and protocols.
Qualifications:
- Ph.D. in Biophysics, Biochemistry, Physics, or a closely related field.
- Minimum of 5 years of post-doctoral research experience in a relevant area of biophysics.
- Extensive hands-on experience with a range of biophysical techniques (e.g., SPR, ITC, CD, fluorescence spectroscopy, NMR).
- Proficiency in experimental design, data acquisition, and advanced statistical analysis.
- Strong knowledge of molecular biology and biochemistry principles.
- Experience with computational modeling and simulation software is a plus.
- Demonstrated success in obtaining research grants and publishing in high-impact journals.
- Excellent leadership, project management, and communication skills.
- Ability to work effectively in a hybrid work environment, balancing remote and on-site responsibilities.
- Experience with assay development and high-throughput screening is advantageous.
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Lead Xenobotanist - Research & Development
00100 Abothuguchi West
KES150000 Annually
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Posted 7 days ago
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Our client is at the forefront of groundbreaking Scientific Research & Development and is seeking a visionary Lead Xenobotanist to spearhead their extraterrestrial flora research division. This role is pivotal in exploring, cultivating, and understanding alien plant life forms, contributing to our client's mission to expand humanity's biological knowledge beyond Earth. The Lead Xenobotanist will design and execute complex research projects, develop novel cultivation techniques for xenobotanical specimens, and analyze their genetic makeup, physiological responses, and ecological impact in simulated environments. This position involves extensive laboratory work, requiring meticulous data collection, advanced statistical analysis, and the interpretation of intricate biological datasets. You will be responsible for establishing and maintaining containment protocols, ensuring the safety and integrity of research operations. Collaboration is key; you will work closely with exobiologists, geneticists, astrobiologists, and environmental scientists to integrate findings and develop practical applications, such as sustainable life support systems for space exploration or novel pharmaceutical compounds. The successful candidate will be proficient in advanced microscopy, sterile techniques, and a range of molecular biology methodologies. Experience with bioinformatics and phylogenetic analysis of novel species is highly desirable. Grant writing and the ability to secure research funding will also be a significant aspect of this role. This position is based in **Nairobi, Nairobi, KE**, offering a hybrid work model, balancing essential in-lab research with remote data analysis and collaboration. The Lead Xenobotanist will mentor junior researchers, publish findings in peer-reviewed journals, and present research at international conferences. A Ph.D. in Botany, Astrobiology, or a related field, with a specialization in plant physiology or molecular biology, is required. A proven track record of leading research projects and managing scientific teams is essential. This is a unique opportunity to make a profound impact on the future of scientific discovery in a rapidly evolving field.
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2
Clinical Research Associate - Pharmaceutical Development
00300 Tuwan
KES280000 Monthly
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Posted 2 days ago
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Job Description
Our client, a leading innovator in pharmaceutical research, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their esteemed, fully remote clinical development team. This crucial role involves overseeing and managing clinical trial activities, ensuring compliance with regulatory standards, and safeguarding the integrity of data collected. The CRA will be responsible for site selection, initiation, monitoring, and close-out activities, acting as a vital liaison between the sponsor and investigational sites. This position requires a strong understanding of Good Clinical Practice (GCP) guidelines, clinical trial protocols, and pharmaceutical research methodologies.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct site visits (remote and/or on-site as required, with travel as needed) to assess protocol and regulatory compliance, data accuracy, and overall site performance.
- Ensure that investigational sites adhere strictly to the study protocol, GCP, and all applicable regulatory requirements.
- Manage communication with clinical investigators and site staff, providing necessary training and ongoing support.
- Review and verify source documents, case report forms (CRFs), and other study-related records for accuracy and completeness.
- Identify, document, and resolve deviations and adverse events promptly and appropriately.
- Assist in the preparation and distribution of study-related documents and essential regulatory documents.
- Track study progress, identify potential risks, and implement mitigation strategies to ensure timely completion of study milestones.
- Participate in investigator meetings and training sessions as required.
- Contribute to the development and refinement of study protocols and clinical research processes.
Qualifications:
- A Bachelor's degree in a life science, nursing, pharmacy, or a related healthcare field. Advanced degree preferred.
- Minimum of 3-5 years of direct experience as a CRA in the pharmaceutical or biotechnology industry.
- Thorough knowledge of GCP, ICH guidelines, FDA regulations, and other relevant regulatory standards.
- Experience in monitoring various phases of clinical trials.
- Excellent organizational skills, with the ability to manage multiple priorities and deadlines effectively.
- Strong written and verbal communication skills, with the ability to document findings clearly and concisely.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and collaboratively in a remote team environment.
- This role supports global initiatives but is specifically aligned with operational oversight relevant to the Eldoret, Uasin Gishu, KE geographical area, requiring adherence to local regulatory nuances.
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3
Clinical Research Associate, Pharmaceutical Development
80200 Shella
KES720000 Annually
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Posted 6 days ago
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Job Description
Our client, a global leader in pharmaceutical innovation, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their dynamic team. This is a fully remote position, enabling you to contribute to groundbreaking research from anywhere in Kenya.
Responsibilities:
Qualifications:
This critical role supports pharmaceutical research relevant to Malindi, Kilifi, KE , and is offered as a fully remote opportunity. If you are a dedicated CRA passionate about advancing medical science, we encourage you to apply.
Responsibilities:
- Plan, implement, and manage clinical trial activities in compliance with Good Clinical Practice (GCP), regulatory requirements, and study protocols.
- Identify, evaluate, and train potential clinical trial sites.
- Monitor clinical trial sites through remote and on-site visits to ensure data accuracy, patient safety, and protocol adherence.
- Ensure proper documentation, record-keeping, and data management for all clinical trial activities.
- Collect, review, and verify clinical data, identifying and resolving discrepancies.
- Communicate effectively with investigators, site staff, study sponsors, and regulatory authorities.
- Prepare and submit regulatory documents and reports as required.
- Manage study supplies and ensure the proper handling and storage of investigational products.
- Participate in site audits and inspections.
- Contribute to the development of study protocols, case report forms (CRFs), and other study-related documents.
- Manage relationships with investigative sites, fostering strong collaborations.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field. Advanced degree is a plus.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
- Thorough understanding of GCP guidelines and regulatory requirements for clinical trials.
- Proven ability to conduct remote monitoring and site management effectively.
- Excellent organizational, analytical, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to communicate complex information clearly.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to work independently, manage multiple priorities, and meet strict deadlines.
- Detail-oriented with a commitment to data integrity and patient safety.
- Experience in specific therapeutic areas is advantageous.
This critical role supports pharmaceutical research relevant to Malindi, Kilifi, KE , and is offered as a fully remote opportunity. If you are a dedicated CRA passionate about advancing medical science, we encourage you to apply.
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4
Clinical Research Associate, Pharmaceutical Development
00100 Gathiruini
KES100000 Annually
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Posted 6 days ago
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Job Description
Our client, a leading pharmaceutical innovator, is actively seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their dedicated drug development team. This is a fully remote position, offering unparalleled flexibility to contribute to critical clinical trials from anywhere. You will be responsible for monitoring clinical trial sites, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Your role will involve data verification, site management, and fostering strong relationships with investigators and site staff. The ideal candidate will possess exceptional organizational skills, meticulous attention to detail, and a comprehensive understanding of clinical trial processes.
Responsibilities:
Qualifications:
Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits for clinical trials.
- Ensure compliance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements.
- Verify accuracy and completeness of source documentation and case report forms (CRFs).
- Manage data queries and ensure timely resolution.
- Communicate effectively with investigators, study coordinators, and site staff.
- Track study progress, including patient recruitment, enrollment, and data collection.
- Identify and report adverse events and protocol deviations.
- Ensure investigational product is managed according to study protocol and regulatory requirements.
- Maintain all study-related documentation in compliance with regulatory standards.
- Contribute to the development of study protocols and clinical trial documents.
- Identify and address site-level issues, escalating as necessary.
- Prepare and present study updates and findings to project teams and management.
- Ensure timely submission of site regulatory documents.
- Promote a positive and collaborative working relationship with clinical trial sites.
- Stay current with industry trends and best practices in clinical research.
Qualifications:
- 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 (CRA) or in a similar clinical trial management role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with various therapeutic areas is a plus.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent monitoring and site management skills.
- Strong analytical and problem-solving abilities.
- Exceptional written and verbal communication skills.
- Ability to travel to clinical sites as needed (though the role is primarily remote, occasional travel may be required).
- High level of organization and attention to detail.
- Ability to work independently and manage time effectively in a remote setting.
- Team player with strong interpersonal skills.
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5
Clinical Research Associate, Pharmaceutical Development
40100 Kisumu
KES320000 Annually
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Posted 7 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 remote clinical development team. This position is a fully remote role, offering the flexibility to manage clinical trials and contribute to life-saving research from anywhere. You will be responsible for monitoring clinical trial sites, ensuring compliance with protocols and regulations, and contributing to the successful execution of clinical studies. The ideal candidate has a strong background in clinical research, excellent organizational skills, and a passion for advancing healthcare.
Key Responsibilities:
Qualifications:
This fully remote role offers a vital opportunity to contribute to groundbreaking pharmaceutical research from anywhere, supporting our operations within Kisumu, Kisumu, KE .
Key Responsibilities:
- Monitor clinical trial sites to ensure adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
- Initiate, monitor, and close-out study sites, including conducting site visits (on-site and remote).
- Verify the accuracy, completeness, and integrity of clinical data collected at study sites.
- Train and support study site staff on protocol requirements, data collection, and regulatory compliance.
- Manage study documentation and ensure the maintenance of regulatory files at sites.
- Communicate effectively with investigators, study coordinators, and other site personnel.
- Identify and report adverse events and protocol deviations promptly.
- Prepare monitoring visit reports and follow up on action items.
- Collaborate with internal teams, including data management, regulatory affairs, and project management.
- Ensure the timely recruitment of subjects according to study targets.
- Contribute to the development of study protocols and clinical trial documentation.
- Stay up-to-date with regulatory changes and industry best practices in clinical research.
- Manage study supplies and equipment at clinical sites.
- Ensure the quality and integrity of data submitted for analysis.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Master's degree is a plus.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- Thorough understanding of GCP guidelines, regulatory requirements (e.g., FDA, EMA), and clinical trial processes.
- Experience with various therapeutic areas is advantageous.
- Excellent monitoring and site management skills.
- Strong attention to detail and data accuracy.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities, with the capacity to manage multiple priorities in a remote setting.
- Ability to work independently and as part of a remote team.
- Willingness to travel as needed for site visits (if applicable to specific role nuances, though the core is remote).
- Problem-solving and critical thinking skills.
This fully remote role offers a vital opportunity to contribute to groundbreaking pharmaceutical research from anywhere, supporting our operations within Kisumu, Kisumu, KE .
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6
Lead Pharmaceutical Research & Development Scientist
80300 Shella
KES130000 Annually
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Posted 3 days ago
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Job Description
Our client, a prominent pharmaceutical entity, is seeking an exceptional Lead Pharmaceutical Research & Development Scientist for a fully remote position. This senior role is pivotal in driving innovation and advancement in drug discovery and development. You will be responsible for leading research projects from conceptualization through to pre-clinical stages, designing and executing complex experiments, and analyzing data to identify promising drug candidates. The ideal candidate possesses a Ph.D. in Pharmacology, Pharmaceutical Sciences, Chemistry, or a related field, with a robust track record of scientific achievement and publications. Responsibilities include mentoring a remote team of researchers, collaborating with cross-functional scientific and clinical teams, and staying abreast of cutting-edge research and regulatory guidelines in the pharmaceutical industry. Experience with drug discovery platforms, analytical techniques, and understanding of regulatory submission processes is critical. You will play a key role in strategic decision-making regarding research pipelines and resource allocation. Strong leadership, project management, and communication skills are essential for effectively managing remote teams and presenting complex scientific findings to diverse stakeholders. We are looking for a highly motivated and visionary scientist dedicated to advancing pharmaceutical science through remote leadership. The geographic operational focus for this role, while remote, pertains to research and development initiatives relevant to the pharmaceutical landscape serving the **Malindi, Kilifi, KE** region and beyond. Your scientific leadership will be crucial in shaping innovative solutions for health challenges. A Ph.D. in a relevant scientific discipline is mandatory, with a minimum of 10 years of post-doctoral experience in pharmaceutical R&D, including significant experience in leading research projects. A proven ability to mentor and guide scientific teams remotely is required.
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7
Senior Pharmaceutical Research & Development Scientist
00100 Abothuguchi West
KES260000 Annually
WhatJobs
Posted 6 days ago
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Job Description
Our client is seeking a highly accomplished Senior Pharmaceutical Research & Development Scientist to join their dedicated, fully remote R&D team. This pivotal role involves leading and contributing to the discovery and development of innovative pharmaceutical products. You will be instrumental in designing and executing preclinical research studies, developing novel drug candidates, and contributing to the early stages of drug development pipelines. The ideal candidate will possess a deep understanding of drug discovery principles, extensive experience in relevant scientific disciplines (e.g., medicinal chemistry, pharmacology, molecular biology), and a proven track record of bringing research projects to fruition. This position requires strong analytical skills, excellent project management capabilities, and the ability to collaborate effectively in a remote, fast-paced environment.
Key Responsibilities:
Qualifications:
This fully remote position offers the unique opportunity to drive pharmaceutical innovation from anywhere and make a profound impact on patient health for our client in Nairobi, Nairobi, KE .
Key Responsibilities:
- Lead and conduct research projects focused on the discovery and development of new pharmaceutical agents.
- Design and execute preclinical studies to evaluate drug efficacy, safety, and pharmacokinetics.
- Develop and optimize in vitro and in vivo experimental models relevant to disease areas.
- Analyze and interpret complex scientific data, drawing sound conclusions and making strategic recommendations.
- Collaborate closely with medicinal chemists, pharmacologists, toxicologists, and formulation scientists.
- Contribute to the development of research strategies and the identification of novel drug targets.
- Prepare high-quality research reports, presentations, and manuscripts for internal and external dissemination.
- Ensure compliance with regulatory guidelines (e.g., GLP) and company SOPs.
- Manage timelines and resources for assigned research projects.
- Stay abreast of the latest scientific advancements and competitive intelligence in the pharmaceutical industry.
- Mentor junior scientists and contribute to team development.
- Identify and evaluate new technologies and research tools to enhance R&D capabilities.
- Contribute to the preparation of regulatory submission documents.
Qualifications:
- Ph.D. in Pharmacology, Medicinal Chemistry, Molecular Biology, Pharmaceutical Sciences, or a related discipline.
- Minimum of 8 years of relevant pharmaceutical R&D experience, with a significant focus on drug discovery and early development.
- Proven expertise in designing and executing preclinical studies, including in vitro assays and in vivo models.
- Strong understanding of drug discovery principles, ADMET properties, and common therapeutic areas.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency with relevant scientific software and data analysis tools.
- Exceptional scientific communication, presentation, and writing skills.
- Ability to manage multiple research projects simultaneously and work effectively in a remote team setting.
- Experience with GLP environments is highly desirable.
- Demonstrated ability to lead research initiatives and mentor junior staff.
- Strong publication record in peer-reviewed journals.
This fully remote position offers the unique opportunity to drive pharmaceutical innovation from anywhere and make a profound impact on patient health for our client in Nairobi, Nairobi, KE .
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8
Junior Mechanical Engineer (Research & Development)
20200 Kapsuser
KES4200 Daily
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Posted today
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Job Description
Our client is seeking a bright and inquisitive Junior Mechanical Engineer to join their Research & Development team on a fully remote basis. This is an exceptional opportunity for an emerging engineer eager to contribute to innovative projects and explore new technologies. You will collaborate closely with senior R&D engineers, assisting in the conceptualization, design, prototyping, and testing of novel mechanical systems and devices. The role demands a strong understanding of mechanical principles, excellent analytical skills, and a proactive approach to problem-solving within a virtual team environment. The ideal candidate is passionate about innovation and eager to learn and grow in a cutting-edge R&D setting.
Responsibilities:
Responsibilities:
- Assist in the research and development of new mechanical concepts and designs.
- Support the creation of detailed 3D models and technical drawings using CAD software.
- Perform engineering analysis, including stress, thermal, and kinematic simulations.
- Collaborate on the design and fabrication of prototypes and experimental apparatus.
- Assist in conducting experiments and testing procedures, collecting and analyzing data.
- Contribute to the documentation of research findings, design specifications, and test results.
- Stay abreast of the latest advancements and technologies in mechanical engineering and related fields.
- Participate in R&D team meetings, brainstorming sessions, and design reviews.
- Troubleshoot and resolve technical challenges encountered during development and testing.
- Ensure all R&D activities are conducted with a focus on safety and efficiency.
- Bachelor's degree in Mechanical Engineering or a closely related field.
- Solid understanding of fundamental mechanical engineering principles.
- Proficiency in 3D CAD software (e.g., SolidWorks, CATIA) is highly desirable.
- Experience with simulation and analysis tools (e.g., ANSYS, MATLAB) is a strong plus.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication abilities in English.
- Ability to work independently, manage multiple priorities, and meet deadlines in a remote setting.
- A curious and innovative mindset with a strong desire for continuous learning.
- Detail-oriented with a focus on accuracy and reliability.
- Must have a reliable internet connection and a suitable remote workspace.
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