Senior Clinical Research Associate

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

📋 Description

• Supervision of Monitoring Duties and Study Execution

• Guarantee the proper execution of clinical trials in alignment with the Study Monitoring Plan (SMP) and relevant laws, GCP, and client standards to meet project objectives, timelines, and quality requirements

• Oversee assigned operational facets for the execution of clinical trial activities at designated investigator sites from site activation to database lock

• Act as the primary liaison for designated investigator sites

• Collaborate with SCP to facilitate investigator site development, coaching, and training of site staff to ensure continuous adherence to protocols and the protection of patients

⛳️ Requirements

• At least 3 years of relevant experience in clinical research site monitoring (preferably 2 years in Oncology)

• Desired therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases

• Experience in global clinical trials

• Must possess fluency in English and the native language(s) of the country in which they will be working

🏝️ Benefits

• Comprehensive understanding of clinical trial methodologies

• Knowledge of ICH/GCP guidelines

• Familiarity with Food and Drug Administration (FDA) regulations

• Adherence to Parexel standards