Similar Jobs
See allTrial Master File Representative
Celerion
UK
Clinical Research
Document Management
Communication
Trial Master Files Representative US Operations
Jobgether
US
Document Management
Clinical Research
Organizational Skills
Trial Documentation Associate I
St. Jude Children’s Research Hospital
US
Clinical Research
Document Management
Regulatory Compliance
TMF Operations Lead
Praxis Precision Medicines
US
ICH-GCP
Regulatory Compliance
TMF Lead/Senior TMF Lead
Precision for Medicine
Europe
Microsoft Office
Veeva Vault
GCP
Key Responsibilities:
- Prepare and maintain Trial Master Files for internal and external studies.
- Create file structure and index contents to meet sponsor specifications.
- Communicate with client sponsors, project managers, and study contacts.
Qualifications:
- Bachelor's degree in a related field such as science, nursing, or biomedical discipline.
- Minimum 1 year of document management experience; clinical research experience preferred.
- Excellent interpersonal and communication skills, highly organized and collaborative.
About Celerion:
- Committed to swift, exceptional clinical research through translational medicine.
- A leader in the clinical research industry with a focus on integrity, trust, and teamwork.
- Offers a remote work environment and equal opportunity employment.
Celerion
Celerion is a clinical research organization that uses translational medicine to accelerate drug development. The company values integrity, trust, teamwork, and respect, and is an equal opportunity employer.