Medical Writer X 2

We are thrilled to unveil an outstanding opportunity with our esteemed client for a  Medical Writer to join an esteemed regulatory writing team specializing in medical device regulatory submissions for a global clientele.

Our client, a dynamic and pioneering regulatory medical consulting company, is committed to delivering premier services in the medical device industry. With a core focus on the assessment and examination of published clinical literature, our client champions innovation and cultivates a culture of collaboration.

• Conduct systematic literature reviews and analyze published clinical data.
• Generate literature review reports for integration into Clinical Evaluation submissions.
• Contribute to drafting Clinical Evaluation Plans, Reports, and other regulatory documents.
• Aid in formulating and executing regulatory strategies.
• Collaborate with clients to comprehend their needs and address queries related to regulatory medical writing.
• Acquire and apply diverse regulatory frameworks to pioneer new products and services.

• Bachelor's degree in a life science field, medical devices, or biomedical science with a grade 2:1 or above.
• Exceptional written English with a keen eye for detail.
• Strong verbal communication skills and ability to thrive within a team setting.
• Familiarity with international regulatory affairs including EU MDD/MDR, FDA, and other pertinent regulations.
• Capability to swiftly grasp new concepts and evaluate scientific data.
• Ability to perform effectively under tight deadlines, both autonomously and collaboratively.
• Legally authorized to work in the UK.
• Proficiency in IT usage, particularly Microsoft Office.

• Flexible working
• Bonuses