This is a fully remote position, open to applicants in Poland, +2 more countries.

📋 Description

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

• Provide suitable reporting and follow-up for all safety incidents reported by site personnel.

• Ensure completeness and compile documentation for regulatory and ethical submissions, including IRB approval, informed consent, and lab certifications.

• Offer relevant updates for site-related documentation for inclusion in the Trial Master File (TMF).

• Conduct feasibility studies and identify potential sites as needed.

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

⛳️ Requirements

• Exceptional interpersonal, oral, and written communication abilities.

• Capacity to contribute as part of a remote team.

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

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

• Completion of a two-year college curriculum or equivalent education/training, along with one year of experience in clinical research or other relevant fields.

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

🏝️ Benefits

• Equal employment opportunities irrespective of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or any other class protected by applicable law.

• Supportive and team-oriented work environment.

• Hands-on, approachable leadership.

• A diverse and inclusive workplace.

• Remote work arrangement.