Site Activation Partner I

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

📋 Description

• Initiate and oversee activities along with the management of essential documents during the startup phase.

• Prepare, validate, and submit regulatory documents for internal assessment.

• Facilitate communication between the client and the ethics committee to obtain necessary approvals.

• Assist investigator sites with local Institutional Review Board (IRB) processes.

• Ensure the maintenance of trial master files and uphold project compliance.

⛳️ Requirements

• A minimum of 2 years of relevant experience in clinical site management.

• Familiarity with clinical research and development processes.

• Basic understanding of medical terminology and Good Clinical Practice (GCP) standards.

• Proficient in computer operations and the Microsoft Office Suite.

• Experience with Clinical Trial Management Systems (CTMS) and Electronic Trial Master Files.

🏝️ Benefits

• Health insurance.

• Retirement plans.

• Paid time off.

• Flexible work arrangements.

• Opportunities for professional development.