We are looking for a "Medical Writer" for one of our global & multinational customer who operates in the medical sector.
JOB DESCRIPTION:
Monitor and review literature, including performing systematic literature searches.
Maintain current in-depth knowledge of the clinical landscape, developments, and
trends to support identified product lines and therapeutic area.
Combine an understanding of scientific and research methodology, medical device
regulations and guidelines, and product knowledge to support global regulatory
submissions (MEDDEV; MDR). This includes participating in and, in some cases, leading
cross-functional teams in the clinical evaluation process and the generation of its
consequent documents. Interaction with regulatory agencies may be required.
Contribute to the development and authoring of technical documentation (SOPs,
medical assessments, etc.) for internal and external use in accordance with regulatory
requirements.
REQUIREMENTS:
Advanced level English and German
Proficiency with Microsoft Office Suite
Strong verbal, written, and presentation skills. Medical writing experience.
Excellent time management skills, ability to work independently, self-motivated, highly
accountable for deliverables and timelines
Effective problem-solving capabilities, solution oriented with the ability to understand,
review, and communicate complex technical concepts concisely and accurately