134 Senior Clinical Research Associate jobs in Nairobi
Lead Clinical Research Associate (CRA)
Posted 20 days ago
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Job Description
Our client, a pioneering pharmaceutical firm, is actively searching for an experienced and dedicated Lead Clinical Research Associate (CRA) to join their expanding research team. This is a fully remote position, enabling you to contribute to groundbreaking drug development from the comfort of your home. As a Lead CRA, you will play a pivotal role in overseeing and managing clinical trial activities, ensuring compliance with regulatory standards, and driving the successful execution of studies. Your responsibilities will include coordinating and monitoring clinical trial sites, performing site visits (pre-study, initiation, routine monitoring, and close-out), ensuring data integrity and accuracy, and verifying adherence to protocols and Good Clinical Practice (GCP) guidelines. You will also be responsible for mentoring and training junior CRAs, serving as a key point of contact for investigators and site staff, and resolving site-level issues promptly. This role demands a deep understanding of pharmaceutical research, regulatory affairs, and clinical trial management. The ideal candidate will possess exceptional organizational, communication, and interpersonal skills, with a proven ability to manage multiple tasks and priorities effectively. Experience in therapeutic areas such as oncology, cardiology, or infectious diseases is highly valued. A strong track record of successful site management and a commitment to quality and patient safety are essential. You will work collaboratively with internal teams, including data management, biostatistics, and regulatory affairs, to ensure seamless trial progression. This remote role requires self-discipline, proactivity, and a results-driven approach. A Bachelor's degree in life sciences, nursing, or a related field is mandatory. Advanced degrees or relevant certifications (e.g., ACRP, SoCRA) are a plus. This is an exceptional opportunity to advance your career in clinical research within a supportive and innovative environment. Be part of a team that is committed to improving global health through cutting-edge pharmaceutical development. Your expertise will directly contribute to bringing life-changing therapies to patients worldwide. Embrace a flexible work model that prioritizes outcomes and professional growth.
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Senior Clinical Research Associate
Posted 21 days ago
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing global health, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their esteemed team. This role offers a unique blend of field and remote work, contributing significantly to the successful execution of clinical trials. You will be responsible for monitoring trial progress, ensuring adherence to protocols, and maintaining the integrity of data collected from study sites. The ideal candidate possesses a deep understanding of GCP, regulatory requirements, and possesses exceptional organizational and communication skills. This is an excellent opportunity for a dedicated CRA to contribute to life-changing therapies within a hybrid work model.
Responsibilities:
Responsibilities:
- Conduct site initiation, monitoring, and close-out visits in accordance with clinical trial protocols and standard operating procedures (SOPs).
- Ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, SOPs, GCP, and all applicable regulations.
- Verify the accuracy, completeness, and validity of data reported by study sites.
- Train and guide site staff on trial-related procedures, documentation, and regulatory requirements.
- Manage communication between study sites and internal project teams.
- Resolve data discrepancies and ensure timely query resolution.
- Review essential documents for completeness and accuracy.
- Identify and report adverse events and protocol deviations.
- Contribute to the development of study protocols and other trial-related documents.
- Ensure timely submission of regulatory documents.
- Manage multiple clinical trial sites simultaneously.
- Prepare site visit reports and follow-up actions.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.
- Minimum of 5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical or biotech industry.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements (e.g., FDA, EMA).
- Proven experience in monitoring clinical trials across various therapeutic areas.
- Excellent understanding of clinical trial processes and documentation.
- Strong critical thinking, problem-solving, and decision-making abilities.
- Exceptional communication, interpersonal, and organizational skills.
- Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to travel to clinical sites as required.
- Demonstrated ability to work independently and as part of a remote/hybrid team.
- Commitment to patient safety and data integrity.
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Clinical Research Associate (Remote)
Posted 20 days ago
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Job Description
Our esteemed pharmaceutical client is actively recruiting a dedicated and experienced Clinical Research Associate (CRA) to join their fully remote global team. This critical role will involve overseeing and managing clinical trials in compliance with Good Clinical Practice (GCP), local regulations, and study protocols. The successful candidate will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring the quality and integrity of data collected. You will serve as the primary liaison between the sponsor and the investigational sites, providing training and support to site personnel. This is a remote-first position, offering significant autonomy and the flexibility to manage your workload effectively from your home office. We are looking for an individual with exceptional organizational skills, a keen eye for detail, and a strong understanding of clinical trial processes. Your responsibilities will include conducting site visits (virtual and potentially on-site as needed), reviewing essential documents, verifying data accuracy, resolving data queries, and ensuring timely reporting of adverse events. You will also be instrumental in identifying and escalating site issues to management. This role requires a proactive and self-driven individual who can work independently while maintaining strong collaborative relationships with research teams and stakeholders. The pharmaceutical industry demands rigorous adherence to standards, and this role is central to ensuring the safety and efficacy of new treatments. Your expertise in pharmaceutical development and clinical research methodologies will be highly valued. This position offers a unique opportunity to contribute to groundbreaking medical advancements while enjoying the benefits of a remote work arrangement. The position is based in Mombasa, Mombasa, KE , but is a fully remote role.
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Remote Clinical Research Associate (CRA)
Posted 11 days ago
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Job Description
Our client is searching for a highly competent and experienced Remote Clinical Research Associate (CRA) to join their innovative pharmaceutical research division. This is a fully remote role, offering the opportunity to contribute to critical clinical trials from the comfort of your home. You will be responsible for monitoring and managing clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and applicable regulatory requirements.
Your primary duties will include site selection, initiation visits, routine monitoring, and close-out visits for clinical trial sites. You will verify the accuracy and completeness of source documents, case report forms (CRFs), and other study-related documentation. This role requires ensuring the safety and rights of study participants are protected at all times. You will also be responsible for identifying and reporting adverse events, and escalating any study-related issues to the appropriate personnel. Maintaining effective communication with investigators, site staff, and internal project teams is paramount. The successful candidate will play a key role in ensuring data integrity and regulatory compliance throughout the trial lifecycle.
We are looking for candidates with a Bachelor's degree in a life science, nursing, pharmacy, or a related field. A minimum of 3-5 years of experience as a Clinical Research Associate is required, with demonstrated experience in monitoring clinical trials according to ICH-GCP guidelines and relevant local regulations. Strong understanding of medical terminology, clinical trial processes, and drug development is essential. Excellent organizational, time management, and problem-solving skills are crucial. The ability to work independently, manage a remote territory effectively, and travel occasionally as needed is also required. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. If you are dedicated to advancing healthcare through meticulous clinical trial oversight, we encourage you to apply.
Your primary duties will include site selection, initiation visits, routine monitoring, and close-out visits for clinical trial sites. You will verify the accuracy and completeness of source documents, case report forms (CRFs), and other study-related documentation. This role requires ensuring the safety and rights of study participants are protected at all times. You will also be responsible for identifying and reporting adverse events, and escalating any study-related issues to the appropriate personnel. Maintaining effective communication with investigators, site staff, and internal project teams is paramount. The successful candidate will play a key role in ensuring data integrity and regulatory compliance throughout the trial lifecycle.
We are looking for candidates with a Bachelor's degree in a life science, nursing, pharmacy, or a related field. A minimum of 3-5 years of experience as a Clinical Research Associate is required, with demonstrated experience in monitoring clinical trials according to ICH-GCP guidelines and relevant local regulations. Strong understanding of medical terminology, clinical trial processes, and drug development is essential. Excellent organizational, time management, and problem-solving skills are crucial. The ability to work independently, manage a remote territory effectively, and travel occasionally as needed is also required. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. If you are dedicated to advancing healthcare through meticulous clinical trial oversight, we encourage you to apply.
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3
Remote Clinical Research Associate (CRC)
Posted 20 days ago
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Job Description
Our client, a prominent pharmaceutical research organization, is seeking a dedicated and experienced Remote Clinical Research Associate (CRC) to support their groundbreaking clinical trials. This is a fully remote position, allowing you to contribute to vital medical research from the convenience of your home office. As a CRC, you will play a crucial role in ensuring the integrity and quality of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The ideal candidate will possess a strong understanding of clinical trial processes, excellent attention to detail, and exceptional communication and organizational skills. You will serve as a key liaison between study sites, sponsors, and regulatory authorities. This role requires the ability to work independently, manage time effectively, and travel occasionally for on-site monitoring visits if required (though the primary role is remote). You will be responsible for site selection, initiation, monitoring, and close-out activities, ensuring participant safety and data integrity throughout the trial lifecycle. Key responsibilities include:
Qualifications:
- Performing remote site monitoring activities, including source data verification and source document review.
- Ensuring adherence to study protocols, GCP, and applicable regulatory requirements.
- Monitoring patient safety and reporting adverse events in a timely manner.
- Training site personnel on study procedures and documentation.
- Conducting remote pre-study, initiation, interim, and close-out visits.
- Reviewing and ensuring the accuracy and completeness of clinical trial data.
- Maintaining effective communication with investigators, site staff, and study sponsors.
- Resolving data queries and ensuring timely resolution of site issues.
- Preparing monitoring reports and providing regular updates to study management.
- Assisting with regulatory submissions and audits.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 4 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- In-depth knowledge of GCP guidelines, FDA regulations, and clinical trial methodologies.
- Proven experience in conducting remote monitoring activities.
- Experience with various clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent analytical and problem-solving skills.
- Strong written and verbal communication skills, with the ability to communicate effectively with diverse stakeholders.
- Exceptional organizational skills and meticulous attention to detail.
- Ability to work independently with minimal supervision and manage time effectively in a remote setting.
- Willingness to travel occasionally for necessary on-site monitoring as per project needs.
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Senior Clinical Research Associate (Pharmacology)
Posted 20 days ago
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Job Description
Our client, a global pharmaceutical leader, is seeking an experienced Senior Clinical Research Associate (CRA) specializing in Pharmacology to join their fully remote clinical operations team. In this critical role, you will be responsible for the monitoring and management of clinical trials, ensuring adherence to Good Clinical Practice (GCP) guidelines, study protocols, and regulatory requirements. You will conduct site visits (virtual and potentially on-site as needed), verify data accuracy, manage study timelines, and ensure patient safety throughout the trial process. The ideal candidate will possess a strong understanding of pharmacological principles and their application in clinical trial design and execution. This position requires meticulous attention to detail, exceptional organizational skills, and the ability to work independently and effectively in a remote setting.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements.
- Verify the accuracy and completeness of clinical trial data.
- Manage study timelines and ensure timely completion of trial milestones.
- Train and support site staff on study procedures and data collection.
- Conduct pre-study, initiation, monitoring, and close-out visits.
- Identify and report adverse events and safety issues promptly.
- Liaise with investigators, study coordinators, and other site personnel.
- Ensure proper documentation and archiving of all study-related materials.
- Participate in the development and review of study protocols and case report forms (CRFs).
- Prepare and submit site monitoring reports.
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5
Senior Clinical Research Associate (Remote)
Posted 18 days ago
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Job Description
Our client is seeking a highly experienced and dedicated Senior Clinical Research Associate (CRA) to join their fully remote clinical operations team. This pivotal role is responsible for ensuring the quality, integrity, and compliance of clinical trials across various therapeutic areas. The ideal candidate will possess extensive knowledge of Good Clinical Practice (GCP), regulatory requirements, and clinical trial processes. You will be tasked with monitoring clinical trial sites remotely, ensuring adherence to study protocols, and verifying the accuracy and completeness of clinical data. This includes conducting site initiation visits, routine monitoring visits (remotely where possible), and site closure activities. A significant part of your role will involve training and supporting site staff, addressing protocol deviations, and resolving any issues that may arise during the trial. You will also be responsible for reviewing case report forms (CRFs), source documents, and other trial-related documentation to ensure data quality and regulatory compliance. Strong communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, site staff, and internal project teams. The successful candidate will have a proven ability to manage multiple studies simultaneously, work independently, and maintain a high level of professionalism and accuracy in a remote setting. This is a remote-first position, requiring exceptional organizational skills, meticulous attention to detail, and the ability to proactively identify and mitigate risks. You will need to be proficient with clinical trial management systems (CTMS) and electronic data capture (EDC) systems. The location for this role, which will be supported remotely, is within the **Mombasa, Mombasa, KE** region.
Key Responsibilities:
Key Responsibilities:
- Perform remote site monitoring visits to ensure adherence to protocols, GCP, and regulatory guidelines.
- Verify the accuracy and completeness of clinical trial data by reviewing source documents and CRFs.
- Train and provide ongoing support to clinical trial site staff.
- Manage site initiation, routine monitoring, and site closure activities.
- Identify, document, and track protocol deviations and adverse events.
- Ensure timely resolution of site issues and data discrepancies.
- Maintain effective communication with investigators, site staff, and internal project teams.
- Prepare monitoring visit reports and ensure follow-up actions are completed.
- Oversee the management of investigational product and study supplies at the sites.
- Contribute to the development of study protocols, monitoring plans, and other trial-related documents.
- Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical or biotechnology industry.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Proven experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent understanding of clinical trial processes and documentation.
- Strong analytical, problem-solving, and organizational skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Ability to work independently, manage time effectively, and meet deadlines in a remote environment.
- Attention to detail and commitment to data integrity and patient safety.
- Experience in multiple therapeutic areas is a plus.
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6
Clinical Research Associate
Posted 20 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical company dedicated to advancing global health, is looking for a dedicated and meticulous Clinical Research Associate (CRA) to join their innovative team. This hybrid role requires a blend of remote work flexibility and on-site presence in Mombasa, Mombasa, KE , offering a unique opportunity to contribute to cutting-edge pharmaceutical development. As a CRA, you will play a crucial role in ensuring the quality, integrity, and efficiency of clinical trials by monitoring study conduct at investigational sites and verifying data accuracy against source documents.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocol, FDA regulations, ICH-GCP guidelines, and other applicable regulatory requirements.
- Verify the accuracy, completeness, and consistency of data entered into the Case Report Forms (CRFs) and electronic data capture systems against source documentation.
- Conduct pre-study, initiation, routine monitoring, and close-out visits to assigned clinical sites.
- Train and support site staff on study protocols, procedures, and regulatory compliance.
- Identify, document, and resolve site-level issues, escalating critical problems to the Clinical Project Manager as needed.
- Ensure all investigational product is managed according to the protocol and accountability logs.
- Review and ensure timely submission of essential regulatory documents.
- Communicate regularly with investigators and site staff to ensure study progress and address any concerns.
- Prepare and submit monitoring reports in a timely and accurate manner.
- Participate in team meetings and contribute to the overall success of the clinical trial program.
- Build and maintain strong working relationships with site personnel and internal stakeholders.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field. A Master's degree is a plus.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- Solid understanding of ICH-GCP guidelines, FDA regulations, and clinical trial processes.
- Experience in monitoring multiple therapeutic areas is advantageous.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills, with the ability to present information clearly and concisely.
- Proficiency in clinical trial databases, EDC systems, and Microsoft Office Suite.
- Ability to travel to assigned sites as required by the hybrid work model.
- Detail-oriented with a commitment to maintaining data integrity and patient safety.
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7
Remote Clinical Research Associate - Pharmaceutical
Posted 19 days ago
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Job Description
Our client, a leading pharmaceutical company focused on developing innovative treatments, is actively seeking a dedicated and meticulous Remote Clinical Research Associate (CRA). In this fully remote role, you will play a crucial part in overseeing and managing clinical trials conducted at various sites, ensuring compliance with protocols, regulations, and good clinical practice (GCP). Your responsibilities will include monitoring trial progress, ensuring data accuracy and integrity, and facilitating effective communication between the sponsor, investigators, and study sites. The ideal candidate possesses extensive knowledge of clinical trial processes, strong regulatory understanding, and excellent organizational and interpersonal skills. You will contribute to bringing life-changing therapies to patients globally, all while working remotely.
Responsibilities:
Qualifications:
Responsibilities:
- Perform remote site monitoring visits and assess protocol compliance.
- Ensure accurate and timely collection, review, and verification of clinical trial data.
- Verify that study participants are enrolled and monitored according to the clinical trial protocol.
- Ensure the rights, safety, and well-being of study participants are protected.
- Train and support investigators and site staff on study procedures and requirements.
- Manage communication between study sites, the sponsor, and other stakeholders.
- Prepare and submit monitoring visit reports and action items.
- Oversee site adherence to GCP, FDA regulations, and other applicable guidelines.
- Track study milestones and timelines, identifying and resolving any potential delays.
- Maintain comprehensive study documentation and regulatory binders.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline.
- Minimum of 3-5 years of experience as a Clinical Research Associate or in a similar clinical research role.
- In-depth knowledge of clinical trial phases, GCP, ICH guidelines, and regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to work independently and travel occasionally if required for specific site visits (though the role is primarily remote).
- Proficiency in Microsoft Office Suite.
- A secure home office environment with a reliable high-speed internet connection.
- Demonstrated ability to manage multiple tasks and prioritize effectively.
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8
Principal Pharmaceutical Scientist (Drug Discovery)
Posted 20 days ago
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Job Description
Our client, a cutting-edge pharmaceutical research and development company, is seeking a highly accomplished Principal Pharmaceutical Scientist to lead groundbreaking drug discovery initiatives. This role is fully remote, offering a flexible and dynamic work environment for talented scientists. You will be responsible for designing and executing novel research strategies to identify and develop new therapeutic agents. Your expertise will span across various stages of drug discovery, including target validation, lead identification, lead optimization, and preclinical development. This position requires a deep understanding of medicinal chemistry, pharmacology, molecular biology, and drug metabolism. The ideal candidate will have a proven track record of success in leading research projects, managing scientific teams, and publishing high-impact research. You will utilize advanced analytical techniques and state-of-the-art laboratory methodologies (where applicable to remote analysis or collaborative lab work). You will also be instrumental in collaborating with internal and external partners, including academic institutions and contract research organizations. This is an exceptional opportunity for a senior scientist to drive innovation and contribute to the development of life-saving medicines. We provide a collaborative and supportive remote work setting that fosters scientific excellence and professional growth. Your ability to think critically, solve complex scientific problems, and communicate research findings effectively will be paramount.
Key Responsibilities:
Key Responsibilities:
- Design and execute comprehensive drug discovery research programs.
- Identify and validate novel drug targets.
- Develop and optimize strategies for lead compound identification and synthesis.
- Conduct pharmacological assays and evaluate drug efficacy and safety.
- Oversee preclinical development studies.
- Analyze and interpret complex scientific data.
- Collaborate with medicinal chemists, biologists, and pharmacologists.
- Prepare research reports, scientific publications, and patent applications.
- Mentor junior scientists and guide research direction.
- Stay abreast of the latest advancements in pharmaceutical sciences and therapeutic areas.
- Ph.D. in Pharmacology, Medicinal Chemistry, Molecular Biology, or a related life science discipline.
- Minimum of 8 years of experience in pharmaceutical research and drug discovery.
- Proven experience in leading complex research projects and scientific teams.
- Extensive knowledge of drug discovery methodologies and technologies.
- Strong publication record in peer-reviewed journals.
- Experience with in vitro and in vivo assay development and validation.
- Excellent analytical, critical thinking, and problem-solving skills.
- Exceptional communication and presentation abilities.
- Demonstrated ability to work independently and lead initiatives in a remote research setting.
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