Senior Site Activation Coordinator – ICF (Informed Consent Form) Locations: Bulgaria | South Africa | Serbia Work Model: Hybrid Make an impact on patient health with IQVIA! Join our Global Site Activation Team, a 2,000‑strong network driving high‑quality
Sr CRA I / II (Phase I Oncology exp a must) Sponsor dedicated Updated: Today Location: Bloemfontein, EC, South Africa Job ID: Description Senior Clinical Research Associate – Phase I oncology. Oversee site preparation, monitoring, and
Job Overview Prepare, maintain, & provide oversight of research-related regulatory documents. Populate & coordinate the entire process for the initial submission of regulatory documents to the IRB, sponsors, & state/ federal regulatory offices, as necessary. Compile
Clinic Care Assistant (Phlebotomist) – Ficksburg (New Store) Dis-Chem Pharmacies Limited Ficksburg, Free State Permanent Closing Date 31 August 2026 Job Details Division Clinic Category Minimum experience Entry Level Company primary industry Retail Job functional area
Main purpose of the job: To identify, screen, and recruit eligible Participants for the TB study within health facilities, ensuring informed and voluntary enrolment, accurate recruitment documentation, and sustained Participant engagement through to completion of study procedures,
Job Overview The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within Bio Pharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol
IQVIA is seeking a Senior Site Activation Coordinator to oversee the development, review, and rollout of Informed Consent Forms across multiple countries in a hybrid work model. You will partner with global and country teams to ensure accuracy,