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

📋 Description

• Oversee the quality of data provided by study sites and ensure timely data submissions.

• Ensure proper reporting and follow-up on all safety incidents as managed by site personnel.

• Guarantee the completeness and organization of regulatory documents and ethical submission materials, including IRB approvals, informed consents, and lab certifications.

• Provide necessary updates for site-related documentation to be filed in the Trial Master File (TMF).

• Conduct feasibility assessments and identify potential study sites as needed.

• Collaborate remotely with colleagues in clinical operations, clients, and sponsor representatives.

⛳️ Requirements

• A four-year degree in a life science field is preferred but not mandatory.

• Completion of a two-year college program or equivalent education/training combined with one year of experience in clinical research (such as study coordinator, CTA, etc.) or other relevant experience is acceptable.

• Exceptional interpersonal, verbal, and written communication abilities.

• Capacity to contribute effectively to a remote team.

• Strong focus on customer satisfaction.

• Ability to interact professionally with sponsor contacts.

• Proficient in Microsoft Office, CTMS, and EDC systems.

• Fluency in English, Bulgarian, and one additional language: German, French, Italian, or Spanish.