Trial Master File Team Member
3 weeks ago
About the Job
We are seeking an experienced Clinical Research Document Coordinator to join our Trial Master File (TMF) Team. As a key member of our team, you will play a crucial role in ensuring the success of our clinical trials by managing and maintaining accurate and compliant documentation.
Key Responsibilities
- Manage and maintain accurate and compliant documentation within the TMF system.
- Ensure that all documents are organized, accessible and meet regulatory standards.
- Collaborate with cross-functional teams to address documentation needs and challenges.
- Contribute to reporting and tracking of TMF deliverables to support project timelines and quality standards.
Benefits
Fortrea offers a competitive salary of $65,000 per annum, plus a range of benefits including health insurance, retirement plan, and paid time off. Our team is passionate about making a meaningful impact on global health, and we are committed to providing opportunities for professional growth and development.
Requirements
To be successful in this role, you will need to have:
- A bachelor's or master's degree in Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field.
- Strong attention to detail and analytical skills, with familiarity in MS Office, especially Excel.
- Proactive, enthusiastic, and eager to learn in a structured environment.
- Excellent communication and organizational skills to manage accuracy-focused tasks and collaborate effectively with cross-functional teams.
About Us
Fortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
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