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

📋 Description

• Ensure the quality of data received from study sites and guarantee timely data submissions.

• Monitor and ensure proper reporting and follow-up for all safety events reported by site personnel.

• Ensure the completeness and compilation of regulatory and ethical submission documentation, including IRB approval, informed consent, and lab certification.

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

• Conduct feasibility studies and identify potential sites as requested.

• Collaborate remotely with clinical operations teams, sponsors, and colleagues across various therapeutic areas.

⛳️ Requirements

• A four-year college degree with a major in life sciences is preferred, but not mandatory.

• A two-year college degree or equivalent education/training along with one year of experience in clinical research (e.g., study coordinator, CTA, etc.) or other relevant experience.

• Outstanding interpersonal, oral, and written communication abilities.

• Capability to effectively contribute to a team in a remote setting.

• Strong customer orientation and the ability to engage professionally with sponsor contacts.

• Proficiency in Microsoft Office, CTMS, and EDC Systems.

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