Gulapro is seeking the services of Clinical Research Associates (CRAs) to serve in anticipated projects and when needed. These positions are highly rewarding and competitive and may not be permanent or physical, may be remote, are contractual, may be short term or long term, renewable and dependent on availability of projects and funds. These positions are open to Kenyan citizens and non-citizens. Should you be interested, please send in your application indicating the position you are applying for in the email subject line to HR@gulapro.com before 15 JUNE 2026.
Please indicate on the application cover letter if you consent to the use of your passport photo and personal professional details for accountability on the Gulapro website upon successful application. Successful applicants will be notified promptly. A Clinical Research Associate manages clinical trial sites, ensuring compliance with protocols, GCPs, and regulations through site selection, initiation, monitoring, and close-out visits. They act as the primary liaison between sponsors and investigators, focusing on data integrity, subject safety, and mentoring less experienced staff
Key Responsibilities
- Site Management: Full ownership of investigator sites through the entire study lifecycle, including site selection, initiation, monitoring, and closure
- Monitoring Visits: Conduct routine interim monitoring and close-out visits to verify adherence to protocols, SOPs, and ICH-GCP guidelines
- Data Verification: Perform Source Document Verification (SDV) to ensure the accuracy and completeness of Case Report Forms (CRFs)
- Regulatory Compliance: Ensure all site regulatory documents (eTMF) are current and complete.
- Investigator Liaison: Act as the primary contact for study site personnel, providing training and support.
Safety Reporting: Verify that all adverse events (AEs) and serious adverse events (SAEs) are reported within mandated timelines. - Study Supplies: Monitor investigational product (medication) accountability and storage.
Mentorship: Provide guidance and training to less experienced CRAs
Required Qualifications & Skills
- Experience: Typically 2–5 years of clinical research experience, with at least 1–2 years of independent
on-site monitoring experience. - Education: Bachelor’s degree in a scientific or health-related field is usually required.
- Knowledge: Strong understanding of ICH-GCP, FDA regulations, and local regulatory requirements
- Skills: Strong communication, organizational, and interpersonal skills; proficient in Microsoft Office
- Travel: Moderate to high travel required (roughly 60%-80% or as required for study monitoring)
Common Performance Metrics
- Meeting monitoring report submission timelines.
- Maintaining study site compliance and data quality standards
- Achieving study recruitment goals