Join IQVIA as a Clinical Research Coordinator!
Are you passionate about clinical research and ready to make a real impact? Do you want to be part of a global leader in healthcare innovation? If so, we’d love to hear from you!
IQVIA is seeking a dedicated Clinical Research Coordinator to join our team in Torpoint, working 24 hours per week on a one year contract. This is a fantastic opportunity to contribute to cutting-edge clinical trials at a single site, supporting investigators and ensuring smooth study operations.
What You’ll Be Doing:
As a key member of the site team, you’ll play a vital role in supporting clinical research activities. Your responsibilities will include:
* Supporting clinical studies in line with health and safety policies under the guidance of the Principal Investigator.
* Maintaining study documentation including protocols, CRFs, and EDC systems.
* Coordinating logistics for study schedules.
* Assisting with data entry, quality checks, and resolving queries to ensure accuracy.
* Supporting patient recruitment and eligibility screening.
What We’re Looking For:
We’re seeking someone who is proactive, detail-oriented, and passionate about clinical research. Ideally, you’ll bring:
* At least 2 years’ experience as a Clinical Research Coordinator, Research Nurse, or Site Research Assistant.
* Solid understanding of clinical trials and study-specific procedures.
* Basic knowledge of medical terminology.
* Strong IT skills, including MS Office (Access, Outlook, Excel, Word).
* Excellent interpersonal and communication skills.
* Strong organisational abilities and attention to detail.
Why IQVIA?
At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research.