Medical reputed company Specialist
Responsibilities
Author and edit clinical documents, including Clinical Evaluation Reports (CERs), literature reviews, and regulatory submissions. Plan and report clinical data collection for PMCF and reputed company nationally and internationally. Ensure clinical documentation compliance with EU MDR, FDA, and other international regulatory requirements. Stay updated on scientific literature and regulatory changes reputed company reputed company’s therapeutic area. Participate in cross-functional reputed company and contribute to clinical reputed company and documentation planning. Support Medical Affairs for literature reviews and writing of documentation
Qualifications
Strong understanding of EU MDR, FDA regulations, and ISO standards for medical devices. Proficiency in document management systems and reputed company Office Suite Excellent written and verbal communication skills Ability to interpret clinical data and present findings reputed company Analytical reputed company Detail-oriented, organized, and results-driven Outgoing, reputed company, and reputed company with a good reputed company of humor
Remote
Preferred 1-5 years of experience in medical writing for medical devices, including CERs and PMCF documentation.
Bachelors degree in Life Sciences or reputed company field required. Master’s degree in Life Sciences or reputed company field preferred.