2,497 Senior Clinical Research Associate Remote jobs in Kenya
Clinical Research Associate - Remote
Posted 22 days ago
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Job Description
Our client is seeking a diligent and experienced Clinical Research Associate (CRA) to join their pharmaceutical research division. This is a fully remote position, offering flexibility while ensuring the highest standards of clinical trial oversight. As a remote CRA, you will be responsible for monitoring clinical trial sites, ensuring adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will conduct site initiation visits, interim monitoring visits, and close-out visits, verifying data accuracy and integrity, and ensuring patient safety. This role requires excellent organizational skills, strong attention to detail, and the ability to communicate effectively with study personnel, investigators, and internal teams. You will play a crucial role in the successful execution of clinical trials, contributing to the development of new pharmaceuticals. The ideal candidate will possess a solid understanding of clinical trial processes, regulatory frameworks, and data management. We are looking for a proactive individual who can manage their workload efficiently and maintain a high level of productivity in a remote setting. This is a significant opportunity to contribute to cutting-edge pharmaceutical research from **Thika, Kiambu, KE**, or any other remote location.
Responsibilities:
Responsibilities:
- Monitor assigned clinical trial sites to ensure compliance with protocols and regulations.
- Conduct site initiation, routine monitoring, and close-out visits.
- Verify the accuracy, completeness, and consistency of clinical data.
- Ensure patient safety and rights are protected throughout the trial.
- Train and support site staff on study procedures and requirements.
- Manage communication between study sites, sponsors, and regulatory authorities.
- Prepare monitoring visit reports and follow up on action items.
- Oversee the collection and management of essential documents.
- Ensure compliance with all relevant ethical and regulatory guidelines (GCP, ICH).
- 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 clinical trial processes, GCP, and regulatory requirements.
- Experience with monitoring clinical trials in relevant therapeutic areas.
- Excellent organizational and time management skills.
- Strong communication, interpersonal, and problem-solving abilities.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and manage travel as needed (if applicable, but focusing on remote capabilities here).
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Lead Clinical Research Associate (Remote)
Posted 13 days ago
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Job Description
Our client, a global biopharmaceutical company, is seeking an experienced and highly motivated Lead Clinical Research Associate (CRA) to join their expanding remote clinical operations team. In this crucial role, you will oversee and manage multiple clinical trial sites, ensuring adherence to Good Clinical Practice (GCP), study protocols, and regulatory requirements. You will play a vital part in the successful execution of clinical studies, from site initiation to close-out.
Key Responsibilities:
Key Responsibilities:
- Conduct pre-study, initiation, interim, and close-out visits for clinical trial sites.
- Monitor trial conduct to ensure adherence to protocol, regulatory requirements, and Good Clinical Practice (GCP).
- Verify the accuracy, completeness, and integrity of clinical data through source document verification.
- Train and mentor site staff on study-related procedures and documentation.
- Manage investigational product accountability and drug destruction.
- Ensure timely data entry and resolution of data queries.
- Build and maintain strong working relationships with investigators, study coordinators, and other site personnel.
- Identify and report adverse events and serious adverse events according to protocol and regulatory guidelines.
- Prepare and submit monitoring reports in a timely and accurate manner.
- Participate in protocol and study-related meetings as required.
- Ensure all site activities are well-documented and maintained in the trial master file (TMF).
- Contribute to the development and review of clinical study protocols and other study-related documents.
- Act as a primary point of contact for assigned sites and internal study teams.
- Provide guidance and oversight to junior CRAs, if applicable.
- Manage site-level recruitment and retention strategies.
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Senior Clinical Research Associate (Remote)
Posted 22 days ago
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Job Description
Our client is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their dynamic research team. This is a fully remote position, offering the flexibility to work from anywhere within Kenya. As a Senior CRA, you will play a critical role in managing and overseeing clinical trials from initiation to close-out. Your responsibilities will include ensuring compliance with Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements. You will be responsible for site selection, initiation, monitoring, and close-out visits, as well as developing and maintaining strong relationships with investigators and site staff. The ideal candidate will possess excellent communication and interpersonal skills, with a proven ability to problem-solve and make sound decisions in a fast-paced environment. You will conduct source data verification, ensure accurate and timely reporting of adverse events, and contribute to the development of study protocols and other essential trial documents. This role requires a meticulous approach to data quality and integrity. You will also be involved in training and mentoring junior CRAs, sharing your expertise and best practices. The ability to manage multiple projects simultaneously and meet strict deadlines is essential. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. We are looking for an individual with a strong scientific background and a deep understanding of the pharmaceutical industry and drug development process. Your commitment to ethical research conduct and patient safety will be paramount. Join a team dedicated to advancing medical treatments and making a significant impact on public health. This role is based in Kericho, Kericho, KE and operates on a remote-first basis, providing significant autonomy and flexibility to the successful candidate. You will be an integral part of a global network, contributing to groundbreaking research initiatives.
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Senior Clinical Research Associate, Remote - Mlolongo
Posted 7 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly experienced and meticulous Senior Clinical Research Associate (CRA) to join their globally distributed team. This is a fully remote position, offering the flexibility to manage clinical trials and ensure data integrity from anywhere. The ideal candidate will possess extensive experience in clinical trial monitoring, regulatory compliance, and site management within the pharmaceutical or biotechnology industry. You will be responsible for overseeing the conduct of clinical trials at investigational sites, ensuring adherence to protocols, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. This role demands exceptional attention to detail, strong organizational skills, and the ability to build effective relationships with site personnel and internal study teams. You will conduct site visits (remote or on-site as required), review source documentation, manage data discrepancies, and ensure timely trial progress. The successful candidate will play a critical role in advancing pharmaceutical research and bringing life-saving therapies to market. This is an outstanding opportunity for a seasoned CRA looking to contribute to impactful drug development programs in a challenging and rewarding remote setting. Experience with various therapeutic areas and clinical trial phases is essential.
Responsibilities:
Responsibilities:
- Plan, implement, and manage clinical trial activities at assigned investigational sites.
- Ensure compliance with study protocols, GCP, FDA regulations, and other relevant guidelines.
- Conduct remote and on-site monitoring visits to assess data accuracy, patient safety, and regulatory compliance.
- Train and support site staff on study procedures, protocol requirements, and data management.
- Review and verify source documents, case report forms (CRFs), and investigational product accountability.
- Identify, document, and resolve site-level issues and deviations.
- Manage communication between the sponsor and investigational sites.
- Contribute to the development of clinical trial documents, such as protocols, investigator brochures, and monitoring plans.
- Oversee site readiness and facilitate study start-up activities.
- Ensure timely submission of all required study documentation and reports.
- Bachelor's degree in a life science, nursing, or related field. Advanced degree preferred.
- 5+ years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in clinical trial monitoring, site management, and regulatory compliance.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent organizational, time management, and communication skills.
- Ability to work independently and effectively manage responsibilities in a remote environment.
- Experience with various therapeutic areas and phases of clinical trials.
- Relevant professional certifications (e.g., ACRP, SoCRA) are a plus.
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Senior Clinical Research Associate - Remote Monitoring
Posted 14 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking a highly diligent and experienced Senior Clinical Research Associate (CRA) to oversee clinical trial activities. This is a fully remote position, allowing you to manage your responsibilities from anywhere while focusing on trials impacting patient populations near Ongata Rongai, Kajiado, KE . You will be responsible for ensuring the quality, integrity, and compliance of clinical trials by monitoring study sites, verifying data accuracy, and ensuring adherence to protocols and regulatory guidelines (e.g., GCP, FDA). The ideal candidate will possess a strong background in clinical trial management, excellent understanding of regulatory requirements, and a keen eye for detail. You will conduct remote site visits, review source documents, resolve data discrepancies, and manage communication between study sites, internal teams, and regulatory authorities. This role requires exceptional organizational skills, a proactive approach to problem-solving, and the ability to work independently and effectively in a remote setting. Experience with various therapeutic areas and electronic data capture (EDC) systems is essential. You will play a crucial role in advancing new therapies through rigorous clinical evaluation, ensuring patient safety and data integrity throughout the process. This is an outstanding opportunity to contribute to significant medical advancements from the convenience of a remote work environment.
Qualifications:
Qualifications:
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 5 years of experience as a Clinical Research Associate.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Proven experience in remote site monitoring and data verification.
- Proficiency with Electronic Data Capture (EDC) systems and clinical trial management software.
- Excellent attention to detail and organizational skills.
- Strong problem-solving and decision-making abilities.
- Effective communication and interpersonal skills for site staff and team collaboration.
- Ability to work independently and manage multiple study sites in a remote capacity.
- Experience in specific therapeutic areas is a plus.
This advertiser has chosen not to accept applicants from your region.
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Clinical Research Associate II (Remote)
Posted 14 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and experienced Clinical Research Associate II (CRA II) to join their dynamic, fully remote clinical operations team. In this critical role, you will play an integral part in ensuring the successful execution of clinical trials according to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. Your primary responsibilities will include remote site monitoring, conducting pre-study, initiation, interim, and close-out visits (where applicable, via remote means or at local sites if needed and permitted). You will be responsible for verifying data accuracy and integrity, ensuring source data verification (SDV), and managing essential study documents. The CRA II will serve as the primary point of contact for assigned investigational sites, building strong relationships with investigators and site staff. You will provide training and ongoing support to site personnel, address protocol-related questions, and ensure timely resolution of site issues. This role requires meticulous attention to detail, excellent organizational skills, and the ability to manage multiple studies and sites concurrently. The ideal candidate will possess strong analytical and problem-solving abilities, coupled with exceptional written and verbal communication skills. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant clinical trial software is essential. As this is a remote position, you must be a self-starter, highly motivated, and capable of working autonomously with minimal supervision. We are looking for individuals with a proven track record in clinical research monitoring and a commitment to patient safety and data quality. This opportunity offers a significant chance to contribute to the development of life-saving pharmaceuticals while enjoying the flexibility of a remote work arrangement. Your dedication to excellence will directly impact the success of our clinical development programs. The role is essential for ensuring compliance and operational efficiency in drug development.
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5
Senior Clinical Research Associate - Remote (Pharmaceutical)
Posted 3 days ago
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Job Description
Our client, a rapidly expanding pharmaceutical company focused on innovative drug development, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join our fully remote global clinical operations team. This critical role will oversee and manage clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The ideal candidate will have a comprehensive understanding of the drug development lifecycle, extensive experience in clinical monitoring, and a proven ability to manage multiple complex clinical trials. Your responsibilities will include conducting site qualification, initiation, interim monitoring, and close-out visits (remotely or in-person as required, but the role itself is remote-based). You will be responsible for verifying the accuracy and completeness of clinical data, ensuring patient safety, and managing site personnel to achieve trial objectives. Strong communication and interpersonal skills are essential for building and maintaining effective relationships with investigators, site staff, and internal project teams. This position requires a meticulous attention to detail, exceptional organizational skills, and the ability to proactively identify and resolve issues. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is mandatory. As this is a fully remote role, you must possess strong self-management capabilities, excellent virtual collaboration skills, and the ability to work independently with minimal supervision. Travel may be required for essential site visits, but the base role is remote. Contributions to study documentation, including protocols, informed consent forms, and study reports, will also be part of your remit. A background in life sciences, nursing, or a related healthcare field, coupled with significant CRA experience, is essential. This is an exceptional opportunity to contribute to life-changing pharmaceutical research from anywhere, supporting global clinical operations that impact patient care worldwide, including potentially near **Nairobi, Nairobi, KE**. Our client offers a competitive salary, comprehensive benefits, and opportunities for professional growth within a cutting-edge pharmaceutical environment.
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Remote Pharmaceutical Clinical Research Associate (Remote CRA)
Posted 16 days ago
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Job Description
Our client is seeking a highly motivated and experienced Remote Pharmaceutical Clinical Research Associate (CRA) to join their growing clinical operations team. This fully remote role will be responsible for monitoring clinical trials, ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. You will conduct site visits (virtually or in-person as needed), assess the quality and integrity of trial data, and ensure patient safety. Key responsibilities include verifying source documentation against case report forms (CRFs), identifying and resolving data discrepancies, and managing investigational product accountability. You will also serve as the primary liaison between the sponsor and study sites, providing training and support to investigators and site staff. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, along with a minimum of 3 years of experience as a Clinical Research Associate in the pharmaceutical industry. A strong understanding of clinical trial processes, regulatory requirements (e.g., FDA, EMA), and GCP is essential. Proven experience in remote monitoring techniques and electronic data capture (EDC) systems is highly desirable. Excellent communication, organizational, and interpersonal skills are required, along with the ability to work independently and manage your time effectively in a remote setting. You must be detail-oriented, proactive, and committed to upholding the highest standards of research integrity. The ability to travel occasionally to sites, if required, should be considered. This is an exceptional opportunity to contribute to the development of life-saving therapies while enjoying the flexibility of a remote work arrangement, supporting our clinical research activities in the Ongata Rongai, Kajiado, KE vicinity.
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Senior Pharmaceutical Clinical Research Associate (Remote)
Posted 21 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking an experienced Senior Pharmaceutical Clinical Research Associate (CRA) to join their fully remote clinical operations team. This role offers the flexibility to manage clinical trials from anywhere, contributing to the development of life-saving medications. You will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The ideal candidate will possess a strong understanding of pharmaceutical drug development processes, clinical trial methodologies, and data management. Your responsibilities will include conducting site initiation visits, routine monitoring visits (including remote monitoring), and site close-out visits. You will review study documentation, verify data accuracy and integrity, and ensure the safety of study participants. This role demands excellent organizational, analytical, and problem-solving skills, as well as exceptional communication and interpersonal abilities to build strong relationships with investigators, site staff, and internal project teams. You will play a crucial part in ensuring the quality and efficiency of clinical trials, contributing to the timely completion of regulatory submissions. A Bachelor's degree in a life science, nursing, or a related field is required; advanced degrees are a plus. Significant experience as a CRA in the pharmaceutical industry is essential. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is a must. You must be a self-motivated, detail-oriented professional capable of managing your workload effectively and making critical decisions independently in a remote environment. This position offers the opportunity to make a significant impact on patient health through rigorous clinical research.
Responsibilities:
Qualifications:
Responsibilities:
- Conduct site visits (remote and on-site if needed) to monitor clinical trial conduct.
- Ensure compliance with study protocols, SOPs, GCP, and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Manage and resolve site-level issues and deviations.
- Review essential documents and source data verification.
- Ensure subject safety and adherence to ethical standards.
- Train and mentor site staff on study procedures.
- Prepare and present monitoring visit reports.
- Build and maintain effective working relationships with investigators and site personnel.
- Contribute to the development of study-related documents.
- Manage assigned trial sites to ensure timely execution and data quality.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 5 years of experience as a Clinical Research Associate in the pharmaceutical industry.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements.
- Experience with various therapeutic areas is advantageous.
- Proficiency in Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems.
- Excellent monitoring and site management skills.
- Strong analytical, problem-solving, and critical thinking abilities.
- Exceptional communication, interpersonal, and negotiation skills.
- Ability to work independently and manage time effectively in a remote setting.
- Detail-oriented and highly organized.
- Willingness to travel occasionally for essential on-site monitoring visits as required.
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8
Senior Clinical Research Associate (CRA) - Remote
Posted 13 days ago
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Job Description
Our client, a leading pharmaceutical company committed to advancing global health, is seeking a highly experienced Senior Clinical Research Associate (CRA) to join their entirely remote clinical operations team. This role offers the flexibility to manage clinical trials from anywhere, contributing to the development of life-changing medicines. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The ideal candidate possesses extensive experience in clinical trial monitoring, strong knowledge of regulatory affairs, and exceptional organizational skills. You will build and maintain strong relationships with investigators and site staff, providing training and support to ensure data integrity and patient safety. We are looking for an individual with exceptional attention to detail, excellent problem-solving abilities, and superior communication and interpersonal skills, capable of thriving in an independent remote work environment. Responsibilities include conducting pre-study, initiation, interim monitoring, and close-out visits, as well as verifying data accuracy and completeness. You will also be involved in resolving site issues, ensuring timely subject recruitment, and preparing monitoring reports. The ability to manage your own schedule, travel as needed (within reasonable parameters for remote roles), and effectively advocate for patient safety and data quality is crucial. This is an exceptional opportunity to contribute to groundbreaking pharmaceutical research while enjoying the autonomy of a remote position. You will be an integral part of a dedicated team focused on bringing innovative therapies to patients worldwide. Our client is committed to professional development and offers a supportive environment for career growth within the pharmaceutical industry.
Responsibilities:
Responsibilities:
- Monitor clinical trial sites to ensure compliance with study protocols, SOPs, GCP, and regulatory requirements.
- Conduct pre-study, initiation, routine monitoring, and close-out visits according to monitoring plan.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Identify, resolve, and escalate site-related issues in a timely manner.
- Build and maintain positive relationships with investigators, site staff, and study teams.
- Provide training and ongoing support to clinical trial site personnel.
- Ensure subject safety and data privacy are maintained throughout the study.
- Prepare and submit comprehensive monitoring reports and follow-up on action items.
- Participate in study team meetings and contribute to study planning and execution.
- Manage a portfolio of clinical trial sites and ensure timely completion of monitoring activities.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. Advanced degree preferred.
- Minimum of 5 years of progressive experience as a Clinical Research Associate (CRA) or equivalent role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in monitoring Phase I-IV clinical trials across various therapeutic areas.
- Exceptional understanding of clinical trial processes and documentation.
- Strong analytical and problem-solving skills, with meticulous attention to detail.
- Excellent written and verbal communication skills, with the ability to effectively communicate with diverse stakeholders.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to travel as required for site visits (typically up to 40-60%, depending on study needs).
- Demonstrated ability to work independently, manage time effectively, and prioritize tasks in a remote setting.
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