- Rhythm Pharmaceuticals (Boston, MA)
- …highly motivated individual to join its team in Boston, Massachusetts. The Associate Director will be the technical lead for Drug Product small molecule ... Responsibilities and Duties + Ensures development and validation of all drug product processes meets regulatory requirements including FDA, EU, ICH requirements… more
- Takeda Pharmaceuticals (Boston, MA)
- … is responsible for supporting the Takeda pipeline programs with expertise in drug product formulation development, process development, drug product ... knowledge. **Job Description** **Objective:** Under the direction of the Director or Sr. Director , ODPD, the Assoc.... drug products for global markets. Expertise in drug product manufacturing process optimization, scale up… more
- Sanofi Group (Cambridge, MA)
- …Prescribing Information, EU SmPC), ensuring alignment with regulatory requirements and Sanofi's product positioning. The Associate Director contributes to ... **Job Title:** Associate Director , Global Regulatory Affairs -...of medicine? The race is on to speed up drug discovery and development to find answers for patients… more
- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... provide medical safety support for safety signal management throughout product lifecycle including signal detection, signal validation, signal escalation,… more
- Takeda Pharmaceuticals (Boston, MA)
- …application is true to the best of my knowledge. **Job Description** ** Associate Director , US Advertising & Promotion Regulatory Review** **Takeda ... Pharmaceutical** **USA-MA-Virtual** **About the role:** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review. Where you will be… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is responsible for ... Global Regulatory Affairs and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple… more
- Takeda Pharmaceuticals (Boston, MA)
- …you and empower you to shine? Join us as a PV Risk Management Scientist/ Associate Director . At Takeda, we are transforming the pharmaceutical industry through ... strive for excellence in everything we do. As an Associate Director / PV Risk Management Scientist, being...strategy to an assigned therapeutic area to ensure that product risk management strategies are consistent worldwide + Provide… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director Global Regulatory Lead, GRAD Oncology. You will provide ... global regulatory strategies in collaboration with their regional counterparts. + As the Associate Director , you will be responsible for complex or highly… more
- Takeda Pharmaceuticals (Boston, MA)
- …leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support ... payers + Identify and prioritize strategic opportunities to enhance and expand product value proposition for new indications Evidence Generation: + Drive evidence… more
- Sanofi Group (Waltham, MA)
- **Job Title:** Associate Director , Genomic Medicine Bioanalytics **Location** : Waltham, MA **About the Job** Are you ready to shape the future of medicine? The ... race is on to speed up drug discovery and development to find answers for patients...our teams accelerate progress. We are seeking a motivated associate director to join our BioAnalytics Characterization… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee the ... of the Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you will contribute:** + Plan, execute and… more
- Takeda Pharmaceuticals (Boston, MA)
- …for the following job opportunity: **JOB LOCATION:** Cambridge, MA **POSITION** : Associate Director , Regulatory Data Governance Lead **POSITION DESCRIPTION** : ... Takeda Development Center Americas, Inc. is seeking an Associate Director , Regulatory Data Governance Lead with the following duties: Oversee the establishment… more
- Takeda Pharmaceuticals (Lexington, MA)
- … Associate Director of Device Clinical Development (DCD) in the Drug Product and Device Development (DPDD) group provides strategic clinical leadership ... for global device and combination product development programs. This pivotal role involves orchestrating device clinical and risk management strategies, establishing… more
- Bristol Myers Squibb (Cambridge, MA)
- …- $193,900 plus incentive cash and stock opportunities (based on eligibility). For the Associate Director position, the starting compensation for this job is a ... upon the early work, additionally exploring mechanisms of resistance, rational drug combinations and product differentiation. The late-stage Translational… more
- Rhythm Pharmaceuticals (Boston, MA)
- …learn, and our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you will be responsible for ... cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs. Responsibilities and Duties + Act...preferred + 8+ years of Regulatory Affairs experience in drug development and product registration activities within… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **_Associate Director , Established Brands Marketing_** **Position Summary** The Associate Director , Established Brands Marketing is responsible for driving ... medical affairs, and finance to implement commercial strategies that sustain product revenue and market positioning. **Key Responsibilities** + **Brand Strategy &… more
- Bristol Myers Squibb (Devens, MA)
- …(CTDO) organization. This Technical Leadership role will provide Technical oversight to drug product and vector sites, covering process validation for commercial ... external manufacturing sites. This role will serve as the Global Technical SME for Drug Product and Vector Validation. The lead will develop global technical… more
- Takeda Pharmaceuticals (Boston, MA)
- …regulatory strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly ... approvals of project(s) of responsibility or oversees direct reports responsible. The Director will lead all submission types. + Accountable for building global… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …effectively and efficiently. **About This Role** We are seeking a strategic, entrepreneurial Associate Director to drive the evolution of OPH's connected health ... experience services. This role requires a unique blend of systems thinking, product vision, and startup grit to translate ambiguous needs into scalable solutions.… more
- Alloy Therapeutics (Waltham, MA)
- …spanning both Alloy and our affiliated venture studio, 82VS. The Role The Associate Director , Strategic Initiatives and Business Operations is a versatile and ... biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to… more