| Within the Methodology and Data Valorization Unit of our R&D and under the supervision of the Pharmacoepidemiology Department Director, we are looking for a: |
Pharmacoepidemiology - Project leader - Permanent contract based in the Head Office in Suresnes, Paris Area
During recent years, we have developed and structured a Pharmacoepidemiology team, with high internal reputation and recognized external network, which is responsible of all international pharmacoepidemiologic studies. The Pharmacoepidemiology Department is based at global R&D HQ and has quickly established a reputation for delivering valuable and pertinent strategic pharmacoepidemiologic studies. The team works on real world studies with particular emphasis on field and database studies of medication safety including risk minimization evaluation (Post-Authorization Safety Studies) and also on a range of studies including epidemiologic knowledge for clinical development and comparative effectiveness for medical affairs purposes across multiple therapeutic areas.
With an important number of drugs in development and planned launches in the following years, and the growing key roles of the real world evidence through the product life cycle, we are expanding the Pharmacoepidemiology Department. Recognized for our high level of expertise and experience in neuropsychiatry, cardiovascular diseases, rheumatology and diabetes, we now aim to develop the oncology field.
We are looking for a candidate with expertise and experience to provide leadership in pharmacoepidemiology and Real World Evidence research. The role will involve internal and external collaboration; working with teams across Therapeutic, Regulatory, Safety, Medical Affairs and Market Access, as well as with external academics and CRO partners.
• Design and conduct retrospective and prospective pharmacoepidemiologic studies; including complex studies, many of them multi-database; • Define the methodology and write protocols; • Write or review statistical analysis plans and other study documents (recruitment plans,…); • Oversee the results, interpret and present the results; • Write and/or contribute to study reports and manuscripts; • Write and/or contribute to Agencies’ scientific documents; • Lead teams/projects with other internal and external research partners; • Scientific collaborations with international experts; participations in professional events and networks.
Joining Servier means working in a stimulating environment and contributing to an innovative, research-based and people-oriented organization. Servier is the leading French independent pharmaceutical company, located in 144 countries with 21000 employees and a turnover of about 4 billion euros in 2015. Around 25% of Servier’s annual turnover is reinvested in Research & Development, reflecting the company’s dedication to its mission of innovation and discovery for improved treatment of unmet medical needs. Organized as a foundation, we guarantee our independence from the stock exchange. Servier is well known for its attention to the wellbeing of the staff, with particular importance placed on career evolution within the Group, and to an agreeable and productive working environment. To know more, visit www.servier.com