PV Manager/Senior PV Manager - Join a fast-growing department
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.
Would you like to be part of a great, growing team responsible for global safety surveillance of Ferring’s portfolio within reproductive health and gastroenterology? Do you thrive in an international environment of great change where you can influence the surroundings?
Do you like to work both with post-marketing and clinical activities?
We are looking for a permanent, experienced Pharmacovigilance Manager with good drive and positive energy.
In Global Pharmacovigilance we are almost 50 international employees responsible for the surveillance of Ferring’s medicinal products and devices. We are organised in two staff functions and three teams. In the Reproductive Health and Gastroenterology team we are currently 10 employees working as Pharmacovigilance Managers and Pharmacovigilance Physicians in dedicated project/product teams. The work in our department is carried out in the mindset of the Ferring Philosophy; trust, integrity, commitment and openness.
As Pharmacovigilance Manager you will play an important role in leading drug safety for a key area of Ferring’s portfolio working as an integrated member of a highly motivated and dedicated team collaborating with clinical development, regulatory affairs, affiliates and partners for assigned products/projects.
Your essential tasks include case processing, post-marketing safety surveillance, safety reports and safety handling in clinical trials in collaboration with Pharmacovigilance Physicians. In addition, as part of the Pharmacovigilance Manager team, you participate in cross functional projects of further development of our processes.
During 2016 we have started up several new clinical trials and internal development projects where your contributions will be essentials.
As a person you are highly motivated, self-driven and able to work in teams. You are flexible, supportive, detail- and action-oriented and keen on working in an international, multi-cultural corporate environment. Good communication skills and fluency in English is essential. Finally, you thrive in a feedback culture.
The preferred candidate has a scientific degree e.g. M Sc Pharm., M Sc Human Biology and with at least 3-5 years of experience from the pharmaceutical industry; experience in pharmacovigilance is mandatory, and experience from regulatory or clinical development will be an advantage. Seniority will be assessed based on the candidate’s qualifications.
Further information about the position can be obtained by contacting Claudia Pierleoni-Nielsen, Director, Reproductive Health and Gastroenterology, Global Pharmacovigilance via mail at email@example.com. Your application and CV in English should be sent as soon as possible but no later than 23 April 2017, as we will be reviewing incoming applications on an on-going basis.