Clinical Trials Coordinator
4 weeks ago
As a leading global contract research organization, Fortrea is dedicated to delivering innovative clinical development solutions to pharmaceutical, biotechnology, and medical device companies. We are seeking a highly motivated and organized Clinical Trials Administrator to join our team.
Key Responsibilities:
- Prepare study site-specific materials in accordance with relevant SOPs
- Set up and maintain clinical investigator files and documentation
- Data entry and maintenance of selected study tracking databases
- Prepare study-related documents and other materials for delivery to archives, at appropriate intervals
- Support payment activities, including preparing invoices, reconciliation, and creating purchase orders
- Perform other administrative duties as assigned
Requirements:
- Life science degree
- Minimum 1 year of clinical trial-related admin experience
- Basic understanding of GCP, ICH Guidelines, and local regulations
- Exceptional administration skills
- Experience in managing multiple priorities and meeting deadlines
- Good social and time management skills
- Good interpersonal skills, oral and written
- General computer literacy in Excel
- Able to work efficiently and effectively in a matrix environment and independently
Working Arrangements:
This role will require the incumbent to work 4 days per week from the client office.
Fortrea is committed to revolutionizing the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. We offer a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
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