Clinical Research Associate I/II

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

📋 Description

• Oversee and take responsibility for the advancement of clinical studies at investigative locations.

• Ensure that clinical trials are executed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and all relevant regulations and standards.

• Organize all essential activities required for setting up and overseeing a study (e.g., identifying investigators, assisting in the preparation of regulatory submissions, conducting pre-study and initiation visits, etc.).

⛳️ Requirements

• A university degree in life sciences, pharmacy, or another health-related field, or equivalent experience in a scientific or healthcare discipline, or be a licensed healthcare professional.

• A minimum of 6 months of experience as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies.

• Experience in site management or equivalent exposure in clinical research.

• Experience in oncology monitoring.

• Strong communication and organizational skills are crucial. Must be a collaborative team player.

• Demonstrated client-focused approach.

• Proficiency in using computerized information systems, electronic spreadsheets, word processing, and electronic mail is required.

• Willingness to travel overnight, with an average of up to 60% travel based on regional requirements. International travel as necessary.

• Fluency in both English and Turkish.

🏝️ Benefits

• Health insurance

• Flexible work arrangements

• Professional development opportunities

• Paid time off