Pharmacovigilance Case Reviewer

Manager, Pharmacovigilance & Medical Information – FranceAbout This Role:As Manager, Pharmacovigilance & Medical Information, you will play a key role in ensuring patient safety and regulatory compliance across Biogen’s pharmacovigilance activities. This position has a unique dual scope, with approximately 50% of the role focused on global...

Manager, Pharmacovigilance & Medical Information - France About This Role: As Manager, Pharmacovigilance & Medical Information, you will play a key role in ensuring patient safety and regulatory compliance across Biogen's pharmacovigilance activities. This position has a unique dual scope, with approximately 50% of the role focused on global...

Individual Consultant for the development of a methodology for investment case analyses of action against AMR in food-producing animals, Veterinary Products and Drug Resistance Department Remote Context The World Organisation for Animal Health (WOAH) is a leading intergovernmental organisation representing 183 Members worldwide. Through its activities, WOAH...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer...

ResponsibilitiesAuthor the Statistical Sections of Protocol.Propose and Review the Study design.Calculate the sample size.Review the Case Report Form (CRF).Review the Edit Check Document (specifically for critical modules like RECIST 1.1 etc.).Write the randomization specifications and coordinate and finalize all the randomization activities with the IWRS...

UNESCO Education Sector is seeking a consultant to deepen understanding of educational exclusion by examining data systems that track out-of-school children and dropout rates. The role includes literature review, country case studies, and developing an EMIS-PATT module to guide capacity-building and policy support.Responsibilities cover desk reviews, remote...

Making preventive health the default for every human in Europe The missionAt the company, we believe healthcare should be preventive, not reactive. We’re building the operating system for human longevity to help people add more healthy years to their lives. The roleLucis analyzes more than 110 biomarkers, builds personalised clinical protocols, and...

Associate Director, Regulatory & Pharmaceutical Affairs (Chief Pharmaceutical Officer Deputy)Paris, FranceThis senior pharmaceutical and regulatory position acts as the trusted right-hand partner (“bras droit”) to the Responsible Pharmacist (RP)/Chief Pharmaceutical Officer (CPO). Working in very close collaboration with the RP/CPO, the role supports the...

Making preventive health the default for every human in EuropeThe missionAt the company, we believe healthcare should be preventive, not reactive. We’re building the operating system for human longevity to help people add more healthy years to their lives.The roleLucis analyses more than 110 biomarkers, builds personalised clinical protocols, and delivers...