Medical / Regulatory Writer

2 weeks ago


Sheffield, United Kingdom Adria Solutions Ltd Full time

Medical Writer - Sheffield. 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.
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.
Familiarity with international regulatory affairs including EU MDD/MDR, FDA, and other pertinent regulations.
Capability to swiftly grasp new concepts and evaluate scientific data.
Proficiency in IT usage, particularly Microsoft Office.
Flexible working
Bonuses


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