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Key Responsibilities:
- Prepare and ensure completeness of Trial Master Files for internal and external studies.
- Maintain the Trial Master File, creating file structure and indexing contents.
- Communicate with client sponsors, project managers, monitors, and sites to ensure compliance.
Qualifications:
- Bachelor's degree in a related field such as science or biomedical discipline.
- Experience in clinical research and/or Trial Master Files preferred.
- Strong interpersonal and written communication skills.
About Celerion:
- A leader in the clinical research industry with a global impact.
- Values include integrity, trust, teamwork, and respect.
- Offers a competitive salary and developmental environment.
Celerion
Celerion is a performance-driven drug research company operating in the clinical research industry. They focus on integrity, trust, teamwork, and respect, offering a strong developmental environment.