Clinical Trial Coordinator
2 weeks ago
Job Summary:
The Clinical Trial Administrator will be responsible for the execution of a Clinical Research Project. This role will involve communicating with project team members, maintaining documentation, and ensuring timely production of high-quality clinical data.
Key Responsibilities:
- Document and track study activities using relevant forms and tools
- Assist in the preparation of study and site-specific materials
- Complete minute-taking and documentation for sponsor/external or internal teleconferences
- Provide support for Investigator Meetings and track meeting attendees
- Maintain Trial Master File documentation and participate in TMF QC
- Audit and CAPA tracking
- Set up and maintain clinical investigator files and documentation
- Liaise with vendors for study conduct
- Coordinate and plan study supply shipments
- Generate reports as needed
Requirements:
- Minimum one year administrative experience or equivalent training
- Good oral and written communication skills
- Good organizational and time management skills
- Computer literacy (Microsoft Office Suite)
About Fortrea:
Fortrea is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions.
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