We are seeking a Senior Clinical Affairs Expert to join a pioneering diagnostics company based in Barcelona .
This is a pivotal role acting as the primary strategic and operational bridge between the company and a leading global CRO, overseeing an ambitious multi-center clinical study across Europe and the USA .
You will be the lead interface for daily operations, ensuring the seamless execution of a large-scale clinical performance study for a novel, breakthrough device.External Partner Management: Act as the primary point of contact for the selected CRO, overseeing site selection, qualification, and training across all sites.Cross-Functional Leadership: Coordinate internal stakeholders across R&D, Marketing, Regulatory, and Quality departments to align clinical strategy.Global Compliance: Ensure study phases strictly adhere to EU IVDR requirements and U.S. FDA regulatory standards.Strategic Oversight: Monitor study progress, identify risks, and implement mitigation actions for a high-volume clinical project.Future Planning: Contribute to the design and planning of post-market clinical follow-up studies.
Education & Training:Bachelor's degree in Life Sciences (Biology, Biotechnology, Pharmacy, Medicine, or similar).An Advanced degree (MSc, PhD, or equivalent) is highly preferred.Specific training in Clinical Trial Management or Regulatory Affairs is a strong asset.
Experience & Skills:Ideally 5–8 years in Clinical Project Management. High-potential candidates with 5–6 years of solid experience are also encouraged to apply.Mandatory experience in Medical Devices, with a strong preference for IVD (In Vitro Diagnostics) .Familiarity with molecular diagnostics, PCR-based assays, or nucleic acid technologies is a plus.Fluent English is essential for daily international coordination.High level of autonomy and excellent stakeholder management skills.