Experienced Study Start-Up Specialist

Our clinical activities are growing rapidly, and we are currently seeking a full-time Regulatory Submissions Coordinator in Greece (home-based) to join our Site Activation & Maintenance deparment. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

• Prepare, review, and file clinical trial applications to domestic regulatory agencies;
• Ensure submissions comply with applicable regulations and guidance documents;
• Advise sponsors and internal stakeholders on changing regulations and compliance requirements;
• Track submissions and ensure timely filing of documents;

• Minimum Bachelor's Degree in Life Sciences;
• At least 2 year of experience as a Study Start-Up Specialist for EC/RA applications in Greece;
• Knowledge of Microsoft® Office;
• Hands-on experience preparing, reviewing, and submitting regulatory documentation; and
• Excellent command of Greek and very good knowledge of English.