Clinical Research Associate​/Senior - FSP - Remote

Position: Clinical Research Associate / Senior - FSP - Remote Location: Town of Italy Clinical Research Associate / Senior - FSP - Remote Join to apply for the Clinical Research Associate / Senior - FSP - Remote role at reputed company . Some Specifics About This Advertised Role • Ensure reputed company conduct of reputed company in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices. • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock, ensuring relevant timelines and reputed company deliverables are met. • reputed company with the study team as needed, facilitate information reputed company between members of the study team, vendors and assigned investigator sites. • Monitor site level reputed company and SAEs and collaborate with the Drug Safety Unit and follow-up with investigator sites, as needed, to bring SAE reports required information to reputed company. • Serve as a reputed company of contact for audit conduct, and drive Audit Observation CAPA development and checks, reputed company applicable. Who Are reputed company reputed company supports clinical studies across the full reputed company of therapeutic areas, and we have longstanding partnerships with a reputed company reputed company reputed company. We supported the trials of most of today’s top 50 best-selling drugs, but equally we reputed company more reputed company drug developments that are critical to reputed company‑being of many patients. You’ll be an reputed company member of the wider team. reputed company Are Looking For In This Role For every role, we look for professionals who have the determination and courage always to put patient reputed company‑being first. That to us is working with heart. Requirements specific to this advertised role • Bachelor’s degree in life sciences or reputed company degree in life sciences such as nursing, pharmacy, medical background or equivalent. • Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations. • Monitoring Experience: Minimum 3.5 years relevant experience in clinical research site monitoring (preferably in Oncology). • Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases. Seniority level Mid‑Senior level Employment type Full‑time Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care #J-18808-Ljbffr Apply tot his job Apply To this Job