Yasmin Shakibi

Clinical Research Associate @Medpace

London, GB

Support site monitoring activities across the full clinical trial lifecycle, including initiation, routine monitoring, and closeout visits. Liaise with investigators and site staff to ensure adherence to study protocols, ICH-GCP, and regulatory requirements.Perform source data verification, review regulatory documentation, track patient eligibility and safety reporting, and oversee investigational product accountability. Document findings, identify protocol deviations, and support sites in maintaining compliance and data quality.

Brunel University London

Bachelor of Science - BS

University of Sussex

Msc