Clinical Trials Coordinator
4 weeks ago
As a leading global contract research organization (CRO), 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.
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.
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 either as a Clinical Trial Associate, Clinical Research Coordinator, Study Coordinator or similar
- 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.
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