Medical Writer
We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.
Job Description
This position is responsible for the creation of scientific and regulatory documents while working with a cross-functional team in accordance with the highest quality standards. The Medical Writer is responsible for performing, preparing, and maintaining Clinical Evaluation Reports for CE technical documentation in accordance with the requirements of the EU Medical Device Regulations (MDR) and related guidance documents (e.g. MEDDEV.2.7./1 Rev. 4). This involves analysing available safety and performance data for medical devices and preparing clinical data documents that support regulatory submissions for the EU, US, and other international markets.
The Medical Writer also assists with writing and reviewing regulatory documents related to the preparation, conduct and reporting of clinical investigations and other PMCF activities.
Responsibilities
- Creation and maintenance of regulatory documents related to clinical data of Haemonetics products (CER, SSCP, PMCF, CRBA) in liaison with other departments
- Plan and execute structured literature searches, identify and analyse relevant clinical data
- Write Clinical Evaluation plans and reports in compliance with applicable regulatory requirements (EU MDR, MEDDEV 2.7/1, MDCG)
- Write study protocols, safety plans and reports in liaison with Medical and Regulatory Affairs
- Support Medical Affairs and Regulatory Affairs in development and execution of regulatory strategies
Required Qualifications
- Bachelor or Master of Science (required) or higher graduate degree (preferred)
- Minimum of 5 years of experience in in the medical device/pharmaceutical industry. 3 yrs in medical/scientific writing
- Manage numerous external vendors and contingent workers (supervisory role)
- Clear, concise scientific style of writing; attention to detail to provide high-quality results
- Affinity to scientific literature and data analyses using state-of-art information technology
- Basic knowledge of biostatistics and medical background/application of Haemonetics products
- Organized and self-driven; project management skills to manage multi-product writing portfolio
- Excellent English language skills, German or other EU language is a plus
EEO Policy Statement
CH-1274 Signy / Signy-Grens / Signy, Switzerland / CH Remote / Signy
