Ferring Pharmaceuticals A/S, Copenhagen, Denmark
Research and Development, Denmark.
Driven by research and a passion for science Ferring Pharmaceuticals is a biopharmaceutical company dedicated to the development of innovative treatments that make a real difference in people’s lives all over the world. Active in the areas of reproductive health, urology, gastroenterology, endocrinology and orthopedics, we develop medicine on the body's own terms. We believe in the power of people and research - and go where ideas and research take us. We are looking for a new colleague to fill a permanent Pharmacovigilance Coordinator position as soon as possible. Are you interested in becoming part of a dynamic team? Do you thrive by working in an international environment? In addition, are you structured and have good planning skills? Then we may just have the right job for you.
In Global Pharmacovigilance (GPV) we are more than 50 international employees responsible for the surveillance of all Ferring medicinal products and devices. In the Case Processing Team, we are a dedicated team of 13 Pharmacovigilance Coordinators, 3 students and some consultants responsible for case processing. We work in close collaboration with partners, internal stakeholders and affiliates.
The work in our team is carried out in the mindset of the Ferring Philosophy; trust, respect, commitment and openness.
You can expect to become an integrated member of a highly motivated and dedicated team collaborating with the therapeutic teams, business support and compliance, PV technology team in Global Pharmacovigilance, Clinical Development, Regulatory Affairs, Authorities, Affiliates and Partners. The role of the Pharmacovigilance Coordinator covers processing of adverse events reported worldwide on Ferring’s marketed products and from clinical trials.
Some of your essential tasks will be:
- case intake, data entry and coding of adverse events
- in line QC check
- correspondence with affiliates, partners and internationally with other departments
You have an educational background as a nurse, pharmaconomist or equivalent with preferably 2-3 years of experience in the Pharmacovigilance area. You take ownership in prioritization of workload both individually and in teams. As a person you are flexible, structured, have an eye for detail and planning and you are a team player. Strong computer skills, good communication skills and fluency in English are essential.
We offer you an interesting and challenging job in a demanding area of the pharmaceutical industry, in an international, multicultural corporate environment with flexible working conditions and good development opportunities.
Further information about the position can be obtained by contacting Birgitte Staun Pallesen, Director, Case Processing, email@example.com. Submit your application and CV in English as soon as possible and no later than 21 March 2018. We will be looking at the incoming applications on an ongoing basis. Please click here to apply.