Clinical Evaluation Consultant

Picture yourself at one of the best places to work, surrounded by teams and people who challenge you, support you, and inspire you to be extraordinary. GBA Key2Compliance offers more than a job. We offer limitless opportunities to make a difference for our customers and improve patient safety. Join us today! Clinical Evaluation Consultant As a Clinical Evaluation Consultant, you will play a key role in delivering high‑quality, MDR‑compliant clinical documentation that enables our clients to bring safe and effective medical devices to market. You will lead and execute clinical evaluation activities across a variety of device classes, supporting manufacturers with robust scientific analyses and clinical strategy. You will collaborate closely with cross‑functional teams, including regulatory affairs, quality assurance, R&D, risk management, and post‑market surveillance, to ensure that clinical evidence is accurate, compliant, and aligned with both regulatory expectations and device‑specific needs. Your ability to manage projects, perform systematic literature reviews, and communicate clearly with stakeholders will be central to success in this role. Your work directly contributes to the safety and performance of medical devices and strengthens our position as a preferred partner for clinical and regulatory support within the life science industry. Your responsibilities •In collaboration with internal teams and clients, plan, coordinate, and write MDR‑compliant Clinical Evaluations, to ensure timely and compliant delivery of all clinical evidence documentation. • Stay up to date with regulatory guidelines, standards, and best practices within clinical evaluation. • Communicate effectively with Notified Bodies and support clients during regulatory interactions. • Contribute to continuous improvement of templates, procedures, and working practices. • (Senior-level consultants) Mentor colleagues, share expertise, and help build internal capability in clinical evaluation. W