Clinical Trial Assistant (CTA) Bogotá, Colombia (Hybrid) At IQVIA, we drive healthcare innovation by combining science, data, and technology. We strongly believe that diversity fuels innovation and that workplace inclusion is both a legal and ethical commitment.
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory
Research Assistant – ProPharma (Onsite, Seville) – Start ASAP Join ProPharma, a global leader in clinical research support, as a Research Assistant at our site based in Seville. This part-time, 24 hours per week contract role is a great opportunity to
IQVIA LLC in Bogotá is looking for a Clinical Trial Assistant (CTA) to provide administrative and operational support in clinical studies. The role involves managing regulatory documentation and coordinating with various teams to ensure compliance with clinical processes.
Clinical Trial Assistant (CTA) – People With Disabilities Bogotá, Colombia (Hybrid) Overview As a CTA at IQVIA, you will provide administrative and operational support in clinical studies, ensuring compliance with ICH‑GCP and clinical operations processes. Responsibilities Organization and
Location: Envíe su CV y cualquier información adicional requerida después de haber leído esta descripción, haciendo clic en el botón de solicitud. Remote (Preference for Barcelona-based) Type: Full-time / Flexible About Us At The/Studio, our vision
This job is open to candidates working remotely from anywhere Schedule: Monday – Friday | 8h per day, of overlap with US Central Time Compensation: $1,250 USD/month for the first 90 days / $1,500 USD/month after