Are you a detail-driven scientific writer with a passion for turning complex clinical data into clear, compelling evidence? We’re partnering with a forward-thinking medical devices company to find a Clinical Evaluation Writer who will play a pivotal role in supporting regulatory success and patient safety across a diverse portfolio on a 6 month contract.

As a Clinical Evaluation Writer, you’ll take ownership of developing and maintaining key clinical and regulatory documentation. You’ll analyse global clinical data, interpret findings, and translate them into robust, compliant reports that support product lifecycle management.

Key Responsibilities
*Collect, review, and interpret clinical data from a range of post-market and clinical follow-up sources
*Produce and maintain Clinical Evaluation Reports and associated documentation
*Manage timelines for ongoing updates across multiple devices
*Develop and refine Clinical Evaluation Plans and safety/performance summaries
*Collaborate with cross-functional teams to identify evidence gaps and support follow-up strategies
*Contribute to Post-Market Surveillance and Post-Market Clinical Follow-Up activities

Requirements
*Proven experience writing Clinical Evaluation Reports for medical devices
*Strong ability to interpret and present clinical data clearly and effectively
*Solid understanding of clinical evaluation processes and regulatory expectations
*Experience critically reviewing scientific literature
*Confident working independently while collaborating across teams
*Strong organisational skills with the ability to manage competing priorities
*Proficiency in Microsoft Word and Excel

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.