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ICON is the world’s largest and most comprehensive clinical research organization, committed to providing top-tier clinical research services. Powered by healthcare intelligence, ICON offers a dynamic environment where professionals can make a significant impact on global health. The company is actively seeking a Senior CRA to join its Clinical Monitoring team in Kenya.
This is an excellent opportunity for an experienced clinical research professional to take full ownership of investigator sites, manage studies from start-up to close-out, and contribute to groundbreaking research, particularly in the fields of Ebola and HIV. The successful candidate will join a diverse and inclusive culture that values talent and high performance.
Job Overview
Job Title: Senior CRA
Location: Home-Based, Kenya
Positions Available: 1
Employment Type: Full Time
Deadline: Not specified
💰 Salary: Competitive (not specified)
Job Summary
The Senior CRA will be responsible for the full management of investigator sites for assigned clinical studies. This includes performing all types of visits, from pre-study to close-out, providing training to site personnel, and assisting with start-up activities. The role requires a minimum of five years of experience in on-site monitoring, with specific expertise in Ebola and HIV trials.
Duties & Responsibilities
Take full ownership of investigator sites for assigned studies.
Manage sites from start-up through close-out, following the clinical monitoring plan.
Build and maintain strong, long-term working relationships with investigative sites.
Apply and adhere to SOPs, the Clinical Monitoring Plan (CMP), and other relevant study guidelines.
Help identify and qualify potential investigators for clinical trials.
Conduct all types of site visits, including pre-study, initiation, routine monitoring, and close-out visits.
Provide initial and ongoing training to site personnel on study protocols and Good Clinical Practice (GCP).
Assist with start-up activities, including essential document review and collection.
Lead and drive regulatory Ethics Committee submissions and follow-up queries.
Support contract and budget negotiations with sites.
Work with the internal team to support the development of country/site-specific informed consent forms.
Ensure all monitoring activities are conducted in compliance with ICH-GCP guidelines and local regulatory requirements.
Maintain accurate records and documentation for all site visits and activities.
Qualifications & Requirements
A minimum of five years of on-site monitoring experience, specifically covering medium-sized studies from start-up through close-out.
Prior experience in investigator site management from a pharmaceutical company or a CRO environment in Kenya.
Specific experience in Ebola and HIV trials is required.
Must hold a degree in an applicable field.
Excellent written and verbal communication skills.
The ability to work to tight deadlines and manage a heavy workload.
Availability to travel at least 60% of the time.
Must possess a valid driving license.
A working knowledge of ICH-GCP guidelines and both local and international regulatory requirements is essential.
Must be based in Kenya.
How to Apply
Interested candidates can apply directly through the ICON careers portal.
Method of Application:
Click on this link to apply: 👉
If you are a driven and experienced Senior CRA with a passion for clinical research, apply now to join ICON and make a difference.
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