Clinical Specialist Consultant (Fully remote)

We are urgently seeking a Clinical Specialist to support a leading medical device company on a fully remote contract through December 2025, with a strong possibility of extension. While this is a remote role, Ireland-based candidates are preferred to align with the client’s team.The successful candidate will be responsible for writing and reviewing Clinical Investigation Plans, performing literature reviews, and developing Clinical Evaluation Protocols in compliance with regulatory and clinical standards.Key Responsibilities:Author and review Clinical Investigation Plans in collaboration with key stakeholders.Conduct detailed literature reviews to support clinical evaluation documentation.Write and maintain Clinical Evaluation Protocols and related technical documents.Requirements:Degree in a life science, medical, or related field.10+ years of experience preparing clinical documentation for medical device submissions.Solid understanding of EU MDR 2017/745 and relevant clinical evaluation guidance.Contract Details:Rate: Competitive hourly ratesDuration: Until December 2025, with potential extension.Location: Fully remote, ideally Ireland-based.