1,466 Research Associate jobs in Kenya
Clinical Research Associate
80101 Nairobi, Nairobi
KES95000 Annually
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Our client, a leading pharmaceutical entity, is actively seeking a dedicated and experienced Clinical Research Associate (CRA) to join their fully remote global team. This critical role will involve the oversight and management of clinical trials, ensuring adherence to protocols, regulations, and ethical standards. You will be responsible for site selection, initiation, monitoring, and close-out activities. Your primary objective will be to ensure the quality, integrity, and accuracy of the data collected during clinical studies, which are vital for the development of new pharmaceuticals. This position requires extensive travel to study sites when necessary, but the core administrative and planning functions are performed remotely. Key responsibilities include:
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is a plus. A minimum of 3-5 years of direct experience as a CRA is required, with a strong understanding of clinical trial phases and methodologies. Excellent knowledge of ICH-GCP guidelines and regulatory affairs is essential. Superior organizational skills, meticulous attention to detail, and strong written and verbal communication abilities are paramount. You must be proficient in clinical trial management systems (CTMS) and electronic data capture (EDC) systems. The ability to work independently, manage your time effectively, and travel as needed is crucial for success in this remote-first role. This is an exceptional opportunity to contribute to life-saving medical advancements from the comfort of your home office, with necessary travel to research locations. We are looking for passionate professionals committed to advancing healthcare through rigorous clinical research. Join our client's esteemed research division.
- Identifying and qualifying potential clinical trial sites.
- Conducting pre-study, initiation, monitoring, and close-out visits.
- Ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Monitoring study conduct, data collection, and patient safety.
- Verifying source data and ensuring its accuracy against the case report forms (CRFs).
- Managing communication between the sponsor and clinical sites.
- Resolving site-level issues and ensuring timely data entry and query resolution.
- Training site personnel on study protocols and procedures.
- Preparing monitoring reports and ensuring all study documentation is accurate and complete.
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A Master's degree is a plus. A minimum of 3-5 years of direct experience as a CRA is required, with a strong understanding of clinical trial phases and methodologies. Excellent knowledge of ICH-GCP guidelines and regulatory affairs is essential. Superior organizational skills, meticulous attention to detail, and strong written and verbal communication abilities are paramount. You must be proficient in clinical trial management systems (CTMS) and electronic data capture (EDC) systems. The ability to work independently, manage your time effectively, and travel as needed is crucial for success in this remote-first role. This is an exceptional opportunity to contribute to life-saving medical advancements from the comfort of your home office, with necessary travel to research locations. We are looking for passionate professionals committed to advancing healthcare through rigorous clinical research. Join our client's esteemed research division.
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Biomedical Research Associate
00200 Abothuguchi West
KES90000 month
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Our client is seeking a skilled and meticulous Biomedical Research Associate to support groundbreaking research in a state-of-the-art laboratory located in **Ruiru, Kiambu, KE**. This role is essential for advancing our understanding and treatment of various diseases. You will be responsible for conducting experiments, collecting and analyzing biological samples, and meticulously documenting all research activities. Key responsibilities include preparing reagents and solutions, maintaining laboratory equipment, and ensuring adherence to strict safety protocols and good laboratory practices (GLP). You will assist in the design and execution of experimental protocols, working closely with principal investigators and senior scientists. Your role will involve performing a range of laboratory techniques such as cell culture, molecular biology assays (PCR, Western blotting), immunoassays, and possibly animal handling if required. Data entry and analysis using statistical software will be a significant part of your duties. You will contribute to the interpretation of experimental results and the preparation of reports and presentations. Maintaining an organized and clean laboratory environment is crucial. You will also be responsible for ordering and managing laboratory supplies and inventory. Collaboration with other research staff and contributing to a positive and productive lab culture are highly valued. A Bachelor's degree in Biology, Biochemistry, Molecular Biology, Biotechnology, or a related life science field is required. A Master's degree is preferred. Previous hands-on experience in a research laboratory setting, preferably within a biomedical or biotechnology context, is essential. Proficiency in common molecular biology techniques and laboratory procedures is mandatory. Familiarity with data analysis software (e.g., GraphPad Prism, R) is desirable. Strong organizational skills, attention to detail, and the ability to follow complex protocols accurately are critical. Excellent teamwork and communication skills are necessary for effective collaboration within the research team. This is an excellent opportunity to contribute to significant scientific discoveries and advance your career in biomedical research.
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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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2
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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Clinical Research Associate
70100 Moiben
KES70000 month
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Posted 2 days ago
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Our client is looking for an experienced Clinical Research Associate to support their pharmaceutical research and development efforts. This role, based in **Garissa, Garissa, KE**, will involve direct involvement in clinical trials, ensuring compliance with protocols and regulatory standards. The successful candidate will be responsible for site monitoring, data collection, and ensuring the integrity and accuracy of trial information. Key duties include recruiting and enrolling study participants, conducting patient visits, administering study-related procedures, and managing study documentation. You will also be responsible for maintaining communication with investigators, study staff, and the sponsor to ensure smooth trial operations. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements. A Bachelor's degree in a life science or healthcare-related field, or equivalent experience, is required. Prior experience as a Clinical Research Coordinator or Associate is highly preferred. Excellent organizational skills, meticulous attention to detail, and strong interpersonal and communication abilities are essential for success in this position. You will play a critical role in advancing pharmaceutical research and bringing new treatments to patients, contributing significantly to our client's mission. This role offers a hybrid work arrangement, balancing on-site responsibilities with remote flexibility.
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4
Legal Research Associate
80200 Nairobi, Nairobi
KES110000 month
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Posted 3 days ago
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Our client, a prestigious international law firm, is seeking a highly diligent and analytical Legal Research Associate to join their remote team. This role is essential for supporting legal professionals by conducting thorough legal research, analyzing case law, and drafting legal memoranda. You will be expected to delve into complex legal issues, identify relevant statutes and precedents, and synthesize information effectively. This is a fully remote position, requiring exceptional attention to detail and the ability to work autonomously. You will play a critical role in strengthening our client's cases and providing expert legal insights.
Key Responsibilities:
Qualifications:
This fully remote opportunity offers a challenging and rewarding career path for a passionate legal professional, providing the chance to contribute to significant legal cases without the need for physical office presence.
Key Responsibilities:
- Conduct comprehensive legal research using various online databases (e.g., LexisNexis, Westlaw) and traditional legal resources.
- Analyze statutes, regulations, case law, and legal precedents relevant to specific legal matters.
- Prepare detailed legal memoranda, briefs, and summaries of findings for attorneys.
- Assist in the drafting of legal documents, pleadings, and contracts.
- Identify and interpret legal issues, providing clear and concise analysis.
- Monitor legal developments and updates in relevant practice areas.
- Organize and maintain legal research files and databases.
- Support litigation teams by gathering evidence and preparing case documentation.
- Collaborate with legal teams to develop case strategies.
- Ensure accuracy and thoroughness in all research and documentation.
- Maintain strict confidentiality of client information.
Qualifications:
- Law degree (LLB or equivalent) from a recognized institution.
- Admitted to practice law or actively pursuing bar admission is a plus.
- Proven experience in legal research and writing.
- Proficiency with legal research platforms and tools.
- Strong analytical, critical thinking, and problem-solving skills.
- Excellent written and verbal communication skills in English.
- High level of accuracy and attention to detail.
- Ability to work independently and manage time effectively in a remote environment.
- Knowledge of various areas of law (e.g., corporate, civil, criminal) is advantageous.
- Strong organizational skills and ability to manage multiple research projects simultaneously.
- Must be proactive and capable of taking initiative to identify research needs.
This fully remote opportunity offers a challenging and rewarding career path for a passionate legal professional, providing the chance to contribute to significant legal cases without the need for physical office presence.
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5
Clinical Research Associate
50101 Kakamega, Western
KES110000 Annually
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Posted 4 days ago
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Our client, a dynamic pharmaceutical company committed to advancing global health, is seeking an experienced Clinical Research Associate (CRA) to join their fully remote clinical operations team. This position is integral to the successful management and execution of clinical trials, ensuring compliance with protocols and regulatory requirements. The CRA will be responsible for site selection and initiation, monitoring study progress, ensuring data integrity, and supporting site staff through remote interactions. Key responsibilities include performing remote site visits and monitoring, reviewing essential documents, managing study timelines, and communicating effectively with investigators, study coordinators, and internal project teams. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines, clinical trial management, and regulatory affairs within the pharmaceutical industry. Previous experience as a CRA or in a similar role within clinical research is essential. Excellent organizational, analytical, and problem-solving skills are required, along with exceptional communication and interpersonal abilities to foster strong relationships remotely. This fully remote role offers the flexibility to work from home and contribute to impactful medical research, supporting trials that may have operational links to **Kakamega, Kakamega, KE**, necessitating remote oversight and data management.
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6
Clinical Research Associate
00200 Moiben
KES15000 Daily
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Posted 4 days ago
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Our client, a leading pharmaceutical company, is looking for a dedicated and experienced Clinical Research Associate (CRA) to join their team in Garissa, Garissa . This hybrid role involves a mix of remote work and on-site visits to clinical trial sites. As a CRA, you will be responsible for monitoring the progress of clinical trials, ensuring that they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. You will play a pivotal role in managing site activities, training site staff, and ensuring data accuracy and patient safety. This is a critical position that requires meticulous attention to detail, strong organizational skills, and the ability to build effective relationships with investigators and study staff. You will travel to investigational sites to verify that all study procedures are being followed correctly and that all necessary documentation is in place. The role demands a comprehensive understanding of regulatory requirements and a proactive approach to problem-solving. Successful candidates will be adept at identifying and addressing any deviations from the protocol or regulatory standards. This is an excellent opportunity for a skilled CRA to contribute to life-saving research within a supportive and growth-oriented environment. If you are passionate about pharmaceutical research, possess excellent interpersonal skills, and are committed to upholding the highest standards of clinical trial conduct, we encourage you to apply.
Responsibilities:
Qualifications:
Responsibilities:
- Initiate, monitor, and close-out clinical trial sites.
- Ensure compliance with protocols, SOPs, and GCP guidelines.
- Verify the accuracy and completeness of study data.
- Manage and train site personnel on study requirements.
- Oversee drug accountability and investigational product management.
- Conduct site visits (remote and on-site) as per the monitoring plan.
- Resolve data queries and address protocol deviations.
- Communicate effectively with study teams, investigators, and regulatory authorities.
- Prepare and submit monitoring visit reports.
- Ensure timely submission of essential documents.
Qualifications:
- 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 GCP, ICH guidelines, and regulatory requirements.
- Proven experience in clinical trial monitoring and site management.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Proficiency in clinical trial management software.
- Ability to travel as required.
- Detail-oriented with strong analytical skills.
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7
Clinical Research Associate
21100 Kapsuser
KES220000 Annually
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Posted 5 days ago
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Our client, a respected entity within the Pharmaceutical industry, is looking for an organized and meticulous Clinical Research Associate to join their team in Kericho, Kericho, KE . This role is integral to the successful execution of clinical trials, ensuring that they are conducted, recorded, and reported in accordance with the study protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. You will be responsible for site selection, initiation, monitoring, and closing out of clinical trial sites. This hybrid role requires regular on-site visits to investigational sites to verify data, ensure compliance, and provide support to study personnel, balanced with remote administrative and reporting tasks. The Clinical Research Associate will also play a key part in training site staff, managing essential documents, and resolving site-level issues. The ideal candidate will possess a strong understanding of clinical trial processes, excellent attention to detail, and exceptional communication and interpersonal skills to build effective relationships with investigators and site staff. A commitment to ethical research conduct and patient safety is paramount. This position offers a dynamic work environment and the opportunity to contribute to the development of new pharmaceutical products.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits.
- Ensure study conduct adheres to protocol, SOPs, and GCP guidelines.
- Verify accuracy and completeness of clinical data and source documents.
- Monitor patient safety and report adverse events.
- Train and support site staff on study procedures.
- Manage essential regulatory documents at study sites.
- Resolve site-level issues and implement corrective actions.
- Communicate effectively with investigators, site staff, and the clinical study team.
- Prepare monitoring reports and follow-up on action items.
Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial role.
- Thorough knowledge of GCP, ICH guidelines, and clinical trial processes.
- Experience with clinical trial monitoring and data verification.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to travel to investigational sites as required.
- Proficiency in clinical trial management software and data entry systems.
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8
Clinical Research Associate
40100 Kisumu
KES150000 Annually
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Posted 5 days ago
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Job Description
Our client is seeking a qualified and dedicated Clinical Research Associate (CRA) to join their dynamic pharmaceutical research team. This hybrid role is instrumental in ensuring the successful execution of clinical trials, adhering to strict protocols, ethical standards, and regulatory requirements. You will be responsible for monitoring clinical trial sites, verifying data accuracy, and ensuring patient safety throughout the study. Key responsibilities include site initiation, routine monitoring visits, site closure activities, and maintaining all study-related documentation. You will also serve as the primary liaison between the study sites and the sponsor, facilitating communication and resolving any issues that arise. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines, clinical trial methodologies, and regulatory affairs. Excellent organizational, communication, and interpersonal skills are essential. This position involves a combination of remote work, allowing for flexibility in planning and reporting, and on-site visits to clinical trial locations, including facilities near Kisumu, Kisumu, KE , as required. A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field is required, along with a minimum of 3 years of experience as a CRA or in a similar clinical research role. Experience with various therapeutic areas is a plus. We are looking for a meticulous and proactive individual with a strong commitment to data integrity and patient well-being. Your role will be crucial in advancing pharmaceutical research and bringing new treatments to patients.
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