In-House Clinical Research Associate I

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

📋 Description

• Guarantee the quality of data received from study sites and ensure timely data submissions.

• Oversee appropriate reporting and follow-up for all safety incidents by site personnel.

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

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

• Conduct feasibility studies and site identification tasks for potential sites as needed.

• Collaborate remotely with colleagues in clinical operations, sponsors, and site personnel.

⛳️ Requirements

• Exceptional interpersonal, verbal, and written communication abilities.

• Capability to effectively contribute to a remote team.

• Strong customer service orientation and professional interaction skills with sponsor contacts.

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

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

• A two-year college degree or equivalent education/training along with one year of experience in clinical research or related fields.

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

🏝️ Benefits

• Equal employment opportunities regardless 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.