DAVID OWERA
- Nairobi, Kenya
- May 12, 2023
Certified clinical research professional with over 1 year of clinical trial experience and 3 years in medical field as qualified and licenced medical doctor. Knowledge of Good Clinical Practice and clinical research skills.
Education
6years undergraduate course in medicine and surgery
Experience
• Designed, reviewed and documented clinical trial subject’s Informed consent
• Prepared and verified documents for phase II/III Metabolic Syndrome
• Performed study Safety monitoring, AE/SAE/SUSAR reporting
• Designed and reviewed Protocol and CRF
• Performed CRA/CRC roles in clinical trials-remotely, subject recruitment and retention strategies
• Performed Site evaluation and site selection visits, site initiation visits, site monitoring visits, clinical trial site management activities, site close-out visit
• Reviewing source data and CRF for completeness,
accuracy and integrity
• Reviewing data queries and listings
• Completion and maintenance of TMF, regulatory compliance, GCP
• Conducting relevant literature review and critical appraisal
of given study topics.
• Providing medical care to study participants
• Reporting on site enrolment, monitoring visits, protocol
deviations and adverse events.