This position requires a strong candidate with expertise in the analysis of medical literature, data from clinical trials and pre-clinical studies, and sound knowledge of applicable regulations and standards. The position will mainly focus on the development of Clinical Evaluation Plans (CEPs) & Clinical Evaluation Reports (CERs). The purpose of this job is to collaboratively develop strategies for the creation of CEPs followed by the development of clinical evaluation reports (CERs) per EU MDR, to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, re-certification and proposed indication/labeling changes.
This position within Medical Communications is fundamental to building credibility and strengthening relationships with healthcare providers, patients, and industry clients, delivering industry-leading services such as call center staffing and medical writing.
Serving as a key link among essential functions, the Scientific Communications Medical Writer ensures the clear, precise, and accessible communication of critical information. By interpreting clinical study results and collaborating with healthcare professionals and cross-functional teams, the medical writer will prepare journal manuscripts and conference materials to support product development and marketing efforts.
This varied role involves writing accurate scientific / commercial copy for a range of printed and computer-based scientific materials from technical manuscripts to congress materials, interactive web projects and sales aids. The candidate will participate in client meetings / teleconferences and attend scientific meetings and participate in pre-meetings, onsite activities and post meeting work as required / appropriate. You should be passionate about communicating science to a variety of audiences and be able to add a creative edge and maintain quality standards.