ARC Regulatory, Belfast-based CRO, seeks a Clinical Lead to drive ARC’s Sponsor Delegation offering for global client companies. You will lead study design, regulatory alignment, and cross-functional coordination to meet timelines and quality targets.
The role requires 3+ years in IVD or device sponsorship, strong knowledge of IVDR, FDA, GCP, ISO standards, and hands-on TMF/eTMF experience. You will manage stakeholder relationships and ensure compliant data collection across regions.
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Clinical Study Lead — IVD Compliance & Strategy in Lisburn employer: ARC Regulatory
As a leading employer in the clinical research field, we offer a dynamic work environment in Belfast that fosters professional growth and development. Our commitment to employee training ensures that you will receive comprehensive support as you transition into the Research Associate role, while our inclusive culture promotes collaboration and innovation. With opportunities for travel and engagement with diverse clinical sites, you will play a vital role in advancing medical device research and making a meaningful impact in the healthcare sector.
