Senior Clinical Research Associate – FSP

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

📋 Description

• Supervision of Monitoring Responsibilities and Study Execution

• Ensure the proper implementation of clinical trials in alignment with the Study Monitoring Plan (SMP) and relevant laws

• Oversee assigned operational elements for execution at investigator sites

• Act as the main contact for designated investigator sites

• Deliver protocol training and respond to protocol-related inquiries from the investigator site personnel as necessary

• Perform onsite, remote/electronic monitoring as required for study site initiation, routine oversight, and study site closure activities

• Collaborate with the Drug Safety Unit and follow up with investigator sites regarding adverse events

• Submit necessary reports and documentation within stipulated timelines

• Identify and address issues at investigator sites within required timelines

⛳️ Requirements

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

• Comprehensive knowledge of clinical trial methodologies, ICH/GCP, FDA, and local country regulations

• Familiarity with disease and technical areas related to clinical studies

• Bachelor's degree in life sciences or a professional qualification in life sciences such as nursing, pharmacy, medical background, or equivalent

• Must be proficient in English and fluent in the native language(s) of the country of employment

🏝️ Benefits

• Health insurance

• Opportunities for professional growth

• Flexible working arrangements

• Paid time off