At a Glance
- Tasks: Lead clinical studies, manage timelines, and ensure compliance across global sites.
- Company: ARC Regulatory, a leader in IVD device studies based in Belfast.
- Benefits: Competitive salary, professional development, and a dynamic work environment.
- Other info: Fast-paced role with opportunities for career advancement.
- Why this job: Make a real impact in the IVD field while working with a passionate team.
- Qualifications: 3+ years in IVD, knowledge of IVDR/FDA/GCP, and TMF/eTMF experience.
The predicted salary is between 63000 - 77000 £ per year.
ARC Regulatory in Belfast is seeking an experienced Clinical Lead to join its Sponsor Delegation project team. You will manage study design, timelines, internal and external stakeholders, and ensure regulatory and quality standards are met across global sites.
The role requires:
- 3+ years in an IVD device setting
- Strong knowledge of IVDR/FDA/GCP
- Hands-on experience with TMF/eTMF processes and GMP-compliant documentation
You will drive compliant study delivery in a fast-paced environment.
IVD Clinical Study Lead — On-Site Belfast employer: ARC Regulatory
As a Pathologist with our company, you will join a dynamic and inclusive team that values diversity and fosters a supportive work culture. We offer flexible remote working arrangements across the UK, ensuring a healthy work-life balance while providing ample opportunities for professional growth and development in a rewarding environment. Our commitment to equal opportunity means that your skills and contributions will be recognised and valued, making this an excellent place to advance your career.
