- Sanofi Group (Cambridge, MA)
- …cross-functional approach with all key business partners (Commercial, Medical, Clinical, Biostats, Regulatory Affairs , Public Affairs ), Market Access (HEVA, ... **Job Title:** Director Global Market Access and Pricing tolebrutinib **Location:**...has granted Breakthrough Therapy designation for tolebrutinib in nrSPMS. Regulatory filing is underway, with submission to the FDA… more
- Bayer (Cambridge, MA)
- …specialists, Translational Sciences, Pharmacometrics, Research, Clinical Development, Regulatory , Medical Affairs and Commercial/Marketing functions. ... **Senior Director Clinical Pharmacology Lead** The Clinical Pharmacology Lead...Pharmacokinetic/Pharmacodynamic including model-based drug development as evidenced by major Regulatory submission experience (eg NDAs, CTDs, INDs), scientific… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Director of Patient Marketing, Hemophilia A, US Rare Blood Disorders **Location:** Cambridge, MA **About the Job** Sanofi's Rare Blood Disorders ... diseases as well as several promising compounds in the pipeline. The Director , ALTUVIIIO Patient Marketing will be responsible for setting the strategic vision,… more
- Takeda Pharmaceuticals (Boston, MA)
- … regulatory requirements and guidelines. + Knowledge of other relevant regional regulatory nuances and requirements. + Knowledge of scientific principles and ... to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development… more
- Takeda Pharmaceuticals (Boston, MA)
- …Japan Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global ... + Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10, EUCAN, GEM… more
- Rhythm Pharmaceuticals (Boston, MA)
- …This individual will collaborate with partners in Supply Chain, Quality Assurance, Regulatory Affairs , Finance and various CRO/CMO's to achieve Rhythm's ... to join its team in Boston, Massachusetts. The Associate Director will be the technical lead for Drug Product...including CMC Drug Substance, Supply Chain Management, Quality, and Regulatory Affairs . + Manages and executes activities… more
- Takeda Pharmaceuticals (Boston, MA)
- …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, ... following job opportunity: **JOB LOCATION:** Cambridge, MA **POSITION** : Medical Director Pharmacovigilance, Rare Disease & PDT **POSITION DESCRIPTION** : Takeda… more
- Takeda Pharmaceuticals (Boston, MA)
- …assessment document + Engages with partner global functions (eg Clinical Science, Med Affairs , Regulatory Affairs , Biostats) to ensure alignment of global ... empower you to shine? Join us as a PV Risk Management Scientist/Associate Director . At Takeda, we are transforming the pharmaceutical industry through our R&D-driven… more
- Sanofi Group (Cambridge, MA)
- …to masterfully coordinate integrated launch workstreams across the enterprise-spanning medical affairs , marketing, sales, value & access, regulatory , patient ... **Job Title:** US Senior Marketing Director , Radioligand Therapy (RLT) **Location** : Cambridge, MA...than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Associate Director , TLL, Renal Rare Disease, is a field-based, customer facing, non-sales position on Otsuka's Rare Renal team focused on enhancing and improving ... The TLL will work closely with cross-functional leaders from Marketing, Medical Affairs , Sales, Key Accounts, Market Access, Patient Access and the Renal Leadership… more