Clinical Research Document Coordinator
6 days ago
About the Role
As a Clinical Research Document Coordinator at Fortrea, you will play a crucial role in ensuring the organization, accessibility and compliance of essential clinical trial documents. You will work closely with our TMF operations and cross-functional teams to uphold the quality, accuracy, and audit readiness of trial documentation.
Your Responsibilities
- Assist in document classification and organization within the TMF system to ensure documents are audit-ready and meet regulatory standards.
- Analyze deliverable metrics to identify trends and areas for improvement in document management.
- Work with TMF operations and other teams to address documentation needs and challenges.
- Contribute to reporting and tracking of TMF deliverables to support project timelines and quality standards.
- Shadow and Support senior team members to understand the strategy behind TMF operations, gaining knowledge and skills in this critical area of clinical research.
What We Offer
We offer a competitive salary of $60,000 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. Our team is dedicated to revolutionizing the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.
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