Clinical Trials Coordinator
5 days ago
As a leading global contract research organization, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.
We are seeking a motivated and detail-oriented Clinical Trials Coordinator to join our team. In this role, you will be responsible for preparing study site specific materials, setting up and maintaining clinical investigator files, and data entry and maintenance of selected study tracking databases.
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
- A keen interest in Clinical Research
- Exceptional administration skills
- Experience in managing multiple priorities and able to meet deadlines
- Good social and time management skills
- Good interpersonal skills, oral and written
- Exhibit general computer literacy in excel
- Efficient and effective work in a matrix environment and ability to work independently
This role will require the incumbent to work 4 days per week from the client office.
Fortrea is a global contract research organization with a passion for scientific rigor and decades of clinical development experience. We are committed to revolutionizing the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.
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