Clinical Research Associate I/II

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

📋 Description

• Oversee and manage the progress of clinical trials at investigative sites, ensuring that they are conducted, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and all relevant regulations and standards.

• Coordinate all essential activities required for the setup and monitoring of a study, which includes identifying investigators, assisting with regulatory submissions, and conducting pre-study and initiation visits.

⛳️ 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.

• Minimum of 6 months of experience as a Clinical Research Associate (CRA) in a Contract Research Organization (CRO) or the pharmaceutical/biotechnology industry, or equivalent relevant experience and/or demonstrated competencies. Experience in site management or similar roles in clinical research is preferred.

• Prior experience in oncology monitoring.

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

• Proven track record of a client-focused approach.

• Proficiency in utilizing 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 needs, including international travel as necessary.

• Fluency in both English and Turkish is essential.

🏝️ Benefits

• Health insurance

• Options for remote work