Pharmacovigilance Officer
Location: NetherlandsSIRE 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 Pharmaceutical organization, based in Noord-Holland Netherlands.
The company focusses on producing safe generic pharmaceuticals and making them available for the world.
ROLE DESCRIPTION
Together with your team you are responsible for making sure all notifications of side effects are shared and documented internally (locally and globally) and to external parties such as partners or authorities. You work according to SOP's, instructions and manuals. The team is also responsible for making appointments with partners on drug safety and risk management.
You work together with different departments such as QA, marketing and medical affairs.
RESPONSIBILITIES
- Coordinate product information updates with partners, stakeholders and authorities
- Work according to SOP's instructions and manuals
- Implement risk management activities and do analysis
- Train colleagues on relevant and changing requirements
- Reconciliation of side effects with other parties
- Make sure internal and external guidelines are being met
REQUIREMENTS
- Bachelor or Master in a medical or pharmaceutical science area
- Experience working with external stakeholders and partners
- Experience with documentation related to pharmacovigilance and SOP's
- A minimum of 1 year experience in pharmacovigilance
- Strong communication skills
- Ability to work both independently as in a team
- Solutionfocussed
- Fluent in Dutch and English (Written and Verbal)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Pascha Groot.
