Join IQVIA as a Clinical Research Coordinator!
Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully.
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.