What Clinical Research Associate Jobs are in Kenya?

Our client, a dynamic Contract Research Organization (CRO) focused on delivering excellence in clinical trials, is seeking a dedicated Senior Clinical Research Associate (CRA) to join their team in **Kericho**. This is a field-based role requiring significant travel to clinical sites across the region. You will play a critical role in ensuring the quality, integrity, and timely execution of clinical studies by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols and regulatory requirements. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) guidelines and extensive experience in clinical trial monitoring. You will be responsible for building strong relationships with investigators and site staff, providing them with necessary training and support. This is an excellent opportunity for an experienced CRA looking to advance their career within a growing organization that values professional development and scientific rigor.

• Conduct on-site monitoring visits to clinical trial sites to verify patient safety, data accuracy, and regulatory compliance.
• Initiate, monitor, and close out clinical study sites according to study protocols and standard operating procedures (SOPs).
• Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
• Verify source data and medical records against case report forms (CRFs) for accuracy and completeness.
• Train and provide ongoing support to site staff, including investigators and study coordinators.
• Manage site issues, resolve discrepancies, and implement corrective action plans as needed.
• Oversee drug accountability and ensure proper handling and storage of study materials.
• Prepare visit reports, follow-up letters, and other essential study documentation in a timely manner.
• Participate in site selection and qualification visits as required.
• Contribute to the development and review of study-related documents, including protocols and CRFs.

• Bachelor's degree in a life science, nursing, or a related field. A Master's degree or equivalent is a plus.
• Minimum of 5 years of experience as a Clinical Research Associate, with demonstrated experience in site monitoring.
• Thorough understanding of clinical trial processes, GCP, ICH guidelines, and relevant regulatory requirements.
• Proven ability to conduct effective monitoring visits and manage multiple clinical trial sites simultaneously.
• Excellent interpersonal, communication, and negotiation skills.
• Strong organizational and time management skills, with meticulous attention to detail.
• Ability to travel frequently (up to 75%) to clinical trial sites.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to work independently and as part of a team in a demanding environment.
• Commitment to maintaining the highest standards of data integrity and patient safety.

• Competitive salary commensurate with experience.
• Performance-based bonus opportunities.
• Company car or travel allowance.
• Comprehensive health, dental, and vision insurance.
• Paid time off and holidays.
• Opportunities for career advancement and professional development.
• Expense reimbursement for travel and accommodation.
• Retirement savings plan.
• Supportive team environment focused on collaboration.

• Conduct on-site and remote monitoring visits to clinical trial sites to ensure protocol compliance, data accuracy, and patient safety.
• Verify the source data and documentation at clinical sites against the Case Report Forms (CRFs).
• Train and provide guidance to site staff on study protocols, procedures, and regulatory requirements.
• Identify, resolve, and escalate site-related issues in a timely manner.
• Ensure timely data entry and query resolution.
• Manage communication between study sites, the clinical operations team, and other stakeholders.
• Participate in the initiation, monitoring, and closure of clinical trial sites.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements.
• Prepare monitoring reports and provide regular updates on site progress and challenges.

• Bachelor's degree in a life science, nursing, or related discipline; advanced degree preferred.
• Minimum of 4 years of experience as a Clinical Research Associate, with a strong understanding of clinical trial conduct.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements in clinical research.
• Experience in monitoring Phase II and/or Phase III clinical trials.
• Proven ability to manage multiple sites and complex projects simultaneously.
• Excellent organizational, communication, and interpersonal skills.
• Proficiency in clinical data management systems and electronic data capture (EDC) platforms.
• Ability to travel to clinical sites as required (approximately 50-60% travel).
• Strong problem-solving skills and attention to detail.
• Experience in infectious disease trials is a significant advantage.

• Conduct site initiation, interim, and close-out monitoring visits according to study protocols and SOPs.
• Verify the accuracy, completeness, and consistency of source documentation and case report forms (CRFs).
• Ensure compliance with Good Clinical Practice (GCP) guidelines, FDA regulations, and other applicable regulatory requirements.
• Manage and resolve data queries in collaboration with site staff and data management teams.
• Train site personnel on study-specific procedures, protocols, and regulatory requirements.
• Oversee study drug accountability and ensure proper storage and handling.
• Identify and report adverse events (AEs) and serious adverse events (SAEs) according to protocol.
• Communicate effectively with investigators, site staff, study sponsors, and internal study teams.
• Prepare monitoring visit reports and follow up on action items in a timely manner.
• Contribute to the development and review of study-related documents, such as protocols and informed consent forms.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Experience in therapeutic areas such as oncology, cardiology, or infectious diseases is a plus.
• Excellent 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 (up to 50% travel may be expected).
• Strong attention to detail and ability to manage multiple priorities effectively.
• Ability to work independently and as part of a remote and on-site team.
• Valid driver's license and reliable transportation.

• Conduct pre-study, initiation, routine monitoring, and close-out visits to clinical trial sites.
• Ensure compliance with study protocols, Standard Operating Procedures (SOPs), GCP, and applicable regulatory requirements.
• Verify the accuracy, completeness, and consistency of clinical data by reviewing source documents.
• Train and support site staff on study-specific procedures and requirements.
• Manage site relationships and facilitate effective communication between sponsors and sites.
• Oversee subject recruitment and retention efforts at assigned sites.
• Resolve data discrepancies and ensure timely resolution of site issues.
• Prepare and submit visit reports and other required documentation in a timely manner.
• Ensure the proper storage and handling of investigational products and study supplies.

• Bachelor's degree in a life science, nursing, pharmacy, or related field.
• Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
• Thorough understanding of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Proven experience in conducting site monitoring visits and managing multiple clinical trial sites.
• Excellent interpersonal, communication, and organizational skills.
• Ability to work independently and manage time effectively.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel frequently to clinical trial sites.
• Strong problem-solving skills and attention to detail.

• Competitive salary and performance-based bonuses.
• Comprehensive medical, dental, and vision insurance plans.
• Paid time off and company holidays.
• Mileage reimbursement and travel expense coverage.
• Opportunities for professional development and certifications.
• Retirement savings plan.
• Flexible hybrid work arrangement.
• Collaborative and supportive team environment.

• Conduct site initiation, interim monitoring, and close-out visits in accordance with clinical trial protocols and Good Clinical Practices (GCP).
• Verify the accuracy, completeness, and integrity of clinical data collected at research sites.
• Ensure compliance with all applicable regulatory requirements, including FDA regulations and ICH guidelines.
• Manage relationships with investigators and site staff, providing training and support as needed.
• Monitor patient safety and report adverse events according to established procedures.
• Review and ensure proper documentation and filing of essential study documents (e.g., source documents, Case Report Forms).
• Communicate effectively with internal project teams, including project managers, data managers, and statisticians.
• Resolve site-specific issues and implement corrective actions to maintain trial progress and data quality.

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3 years of experience as a Clinical Research Associate, with a proven ability to conduct monitoring visits.
• Thorough understanding of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Experience in therapeutic areas such as oncology, cardiology, or infectious diseases is a plus.
• Excellent organizational and time management skills.
• Strong written and verbal communication skills.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to clinical sites as required by the study.

• Conduct pre-study, initiation, routine monitoring, and close-out visits to clinical trial sites.
• Verify the accuracy and completeness of clinical trial data by comparing it to source documentation.
• Ensure adherence to the study protocol, regulatory requirements (GCP, ICH), and company SOPs.
• Manage site-level activities, including subject recruitment, informed consent process, and regulatory binder maintenance.
• Identify, document, and resolve site-specific issues and deviations.
• Train and support site staff on study procedures and regulatory compliance.
• Communicate effectively with investigators, site staff, project managers, and sponsors.
• Prepare and present monitoring visit reports in a timely manner.
• Track and manage site supplies and investigational product accountability.
• Ensure timely entry of data into clinical trial management systems (CTMS).

• Bachelor's degree in a life science, nursing, or related field.
• Minimum of 3-5 years of experience as a Clinical Research Associate (CRA), with proven experience in site monitoring.
• Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
• Experience in one or more therapeutic areas (e.g., oncology, cardiology, infectious diseases).
• Excellent verbal and written communication skills.
• Strong organizational and time management skills, with the ability to manage multiple sites and priorities.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to travel to clinical sites as required (estimated 50-60% travel).
• Must be able to work effectively both independently and as part of a hybrid team.
• Attention to detail and a commitment to data integrity and patient safety.

• Competitive salary with performance-based incentives.
• Hybrid work arrangement offering a blend of remote flexibility and on-site engagement.
• Comprehensive health, dental, and vision insurance plans.
• Paid time off, including vacation, sick leave, and holidays.
• Opportunities for professional development and career advancement within a growing CRO.
• Travel allowance and per diem for site visits.
• Exposure to diverse therapeutic areas and cutting-edge clinical research.
• Supportive team environment and experienced leadership.
• Company-provided laptop and mobile phone.

Our client, a leading innovator in the pharmaceutical sector, is seeking a highly experienced and dedicated Senior Clinical Research Associate to join their dynamic, fully remote team. This pivotal role offers an exceptional opportunity to contribute to groundbreaking research and development from the comfort of your home office. The successful candidate will play a crucial role in ensuring the efficient and compliant execution of clinical trials, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. This position is ideal for a proactive professional who thrives in a remote-first environment, possesses excellent organizational skills, and has a passion for advancing medical treatments. The role demands a meticulous approach to data management and a strong understanding of the drug development lifecycle. We are looking for an individual who can independently manage complex projects and collaborate effectively with cross-functional teams located globally. The pharmaceutical industry is rapidly evolving, and this role is at the forefront of that change, requiring adaptability and a commitment to continuous learning.

• Oversee and manage all aspects of clinical trial conduct at assigned sites, ensuring adherence to protocols, regulatory requirements, and company SOPs.
• Conduct site initiation, interim monitoring, and close-out visits, either remotely or in-person as required by study needs and company policy.
• Perform source data verification (SDV) and ensure the accuracy, completeness, and integrity of clinical trial data collected.
• Train and mentor site staff on study procedures, regulatory compliance, and data reporting requirements.
• Act as the primary liaison between the investigative sites, the clinical operations team, and other relevant departments.
• Prepare and present site monitoring reports, identifying potential issues and proposing corrective actions.
• Manage investigational product accountability and ensure compliance with drug storage and handling procedures.
• Contribute to the development and review of study-related documents, including protocols, case report forms (CRFs), and informed consent forms.
• Ensure timely resolution of data queries and follow-up on action items from site visits and team meetings.
• Stay updated on relevant therapeutic areas, clinical trial methodologies, and regulatory guidelines to ensure best practices are implemented.

• Bachelor's degree in life sciences, nursing, pharmacy, or a related scientific field. Advanced degree (Master's, PhD) is a plus.
• Minimum of 5 years of experience as a Clinical Research Associate (CRA) in the pharmaceutical or biotechnology industry.
• Proven experience in managing multiple clinical trials simultaneously, preferably in a remote setting.
• In-depth knowledge of ICH-GCP guidelines, FDA regulations, and other applicable regulatory requirements.
• Strong understanding of clinical trial processes from site selection through study close-out.
• Excellent communication (written and verbal), interpersonal, and presentation skills.
• Proficiency in using electronic data capture (EDC) systems, clinical trial management systems (CTMS), and other relevant software.
• Ability to work independently, demonstrate strong problem-solving skills, and manage time effectively in a remote work environment.
• Willingness to travel for essential site visits or training as required (though the role is predominantly remote).
• Detail-oriented with a commitment to accuracy and data integrity.

Our client offers a competitive compensation package, including a comprehensive health insurance plan, retirement savings options, and generous paid time off. Employees benefit from a flexible remote work arrangement, allowing for a healthy work-life balance. Continuous professional development is encouraged through access to training programs, conferences, and opportunities for career advancement within the organization. You will be part of a supportive and collaborative team dedicated to making a significant impact in global health. Opportunities for bonuses based on performance are also available. This role provides the chance to work with cutting-edge technologies and contribute to life-saving therapies, all while maintaining the flexibility of a remote position. We invest in our employees' well-being and professional growth, fostering a culture of innovation and excellence. The company is committed to diversity and inclusion, ensuring a supportive environment for all team members.