Senior Clinical Research Associate I – FSP

This is a fully remote position, open to applicants in Turkey.

📋 Description

• Ensure the appropriate execution of clinical trials in line with the Study Monitoring Plan (SMP) and relevant regulations.

• Oversee the operational elements associated with the execution of clinical trial activities from site activation to database lock.

• Act as the main point of contact for designated investigator sites throughout the study's progress.

• Perform onsite and remote monitoring for site initiation, routine oversight, and closure activities.

• Track adverse events at the site level and work in conjunction with the Drug Safety Unit.

• Submit all necessary reports and documentation within specified deadlines.

• Identify and address issues at investigator sites and devise corrective action plans.

⛳️ Requirements

• At least 3 years of relevant experience in clinical research site monitoring, with a preference for 2 years in Oncology.

• Preferred therapeutic expertise in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.

• Experience in global clinical trials.

• Proficiency in English is essential.

• Willingness to travel extensively throughout Turkey.

• A valid driver’s license and passport are required.

🏝️ Benefits

• Health insurance.

• Opportunities for professional development.

• Option for remote work.