Post Marketing Surveillance Consultant
Location: FranceSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Rhône France.
Worldwide key player in the Medical industry. Portfolio: Class 2b & 3
ROLE DESCRIPTION
The Consultant responsible for Postmarketing surveillance will monitor the safety of the released Medical Device portfolio (Class 2b & 3).
RESPONSIBILITIES
The main purpose of this role is monitoring the device safety.
- Build relationships with KOL, patients and other key players
- Write reports
- Review of electronic health records
- Investigate patient complaints
- Determine the link between the complaints and the medical device
REQUIREMENTS
- IMMEDIATE AVAILABILITY
- Being self-employed (own company)
- Relevant experience
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.