The Position 
Are you passionate about patient health and safety? If yes, we have an exciting opportunity for you!
 
Our dedicated Patient Safety teams are seeking experienced (Senior) Patient Safety Physicians to join us on our journey. You'll have the chance to work on a variety of products, either in clinical development or post-marketing drug safety. We're particularly interested in physicians with expertise in Oncology. If you're ready to take on this challenge and make a real difference in patient safety, we look forward to receiving your application!
 
Tasks & Responsibilities 

In this role as a (Senior) Associate Director / (Senior) Patient Safety Physician for Oncology, you will lead or contribute to the global Patient Safety and Pharmacovigilance (PSPV) and Risk Management (RM) activities for compounds in clinical development or in the market.

In more detail, your tasks may include:

Develop/ contribute to proactive patient-centric RM strategies for assigned compounds.Plan, manage/ perform and monitor all PV activities for assigned drugs, including:Set-up of safety analyses in the clinical trial and safety databases for monitoringContinuous monitoring and further development of the product safety and benefit/risk profileSafety issue managementCollaborate with various departments, including Clinical Development and Global Patient Engagement, to develop patient-centric benefit-risk profile assessment strategies for developmental compounds.Work with Global Epidemiology and Medical Affairs to develop safety-focused post-authorisation studies.Interpret clinical trial safety data for clinical trial reports and submission documentsReview and provide medical-scientific input to regulatory documents (e.g. IBs, PSURs, DSURs, RMPs, Clinical Overview Statements).Update senior management on the assigned drug’s safety profile as requested and recommend PV/ RM activities to BI decision-making bodies. For the Senior position, these would be additional responsibilities:Chair BI-internal multidisciplinary Asset Benefit Risk TeamRepresent PSPV in internal and external committees & bodiesContribute to the further development of PSPV within BI by staying abreast of state-of-the-art methodology, changes in the regulatory environment and developments and trends in healthcare system and society
Requirements Medical Doctor with clinical and/or clinical research experiencePV experience and good understanding of PV regulation in major marketsPV experience in Clinical Development and submissions for marketing authorizsation would be an assetClinical or clinical research experience in OncologyGood interpersonal and communication skillsStrong ethical sense combined with quality and patient safety mindsetExcellent English skills, both written and spokenAbility to handle ambiguity and present complex situations clearly to generate implementation solutions
For the Senior position, you need to meet the additional requirements:Profound experience in PSPV and Risk Management in a pharmaceutical company on a global / corporate level, including clinical development and post-marketing safetyVery good and broad understanding of the pharmaceutical industry, and the future trends and developments in pharmacovigilanceThorough understanding of PV regulation in major markets and respective need for complianceProject Management and leadership competenciesBoard certification in Internal Medicine and/or Medical Oncology would be a plus 
Ready to contact us?  
If you have any questions about the job posting or process - please contact our HR Direct Team, Tel: +49 (0) 6132 77-3330 or per mail: hr.de@boehringer-ingelheim.com 
Please submit your application documents in English.