Clinical Research Associate - Remote

Overview

The Clinical Research Associate will oversee the initiation, monitoring, and closing of clinical trials, ensuring compliance with GCP and regulatory requirements.

In Short

• Oversee clinical trials in compliance with GCP and regulatory requirements.
• Perform on-site and remote monitoring visits.
• Manage investigator sites and ensure proper study conduct.
• Conduct source data verification and ensure accurate data collection.
• Assist in the preparation of study documentation.
• Maintain effective communication with investigators and site staff.
• Resolve data queries and discrepancies.
• Provide training and support to site staff.
• Contribute to regulatory document submissions.
• Collaborate with cross-functional teams.

Requirements

• Proven experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes and GCP.
• Strong organizational and time-management skills.
• Excellent communication and interpersonal skills.
• Ability to travel extensively within Turkey.
• Fluency in English and Turkish.
• Degree in life sciences, pharmacy, or related field.

Benefits

• Opportunity to contribute to impactful clinical research.
• Dynamic and fast-paced work environment.