- Medtronic (Boston, MA)
- …best practices, test automation strategies, and emerging technologies relevant to medical device software. + Champion and implement Lean-Scaled Agile Framework ... coverage and efficiency. + Ensure all software verification activities adhere to relevant medical device regulations (eg, FDA 21 CFR Part 820, ISO 13485, IEC 62304)… more
- Sanofi Group (Cambridge, MA)
- …collecting valuable data, managing budgets and timelines + work with medical leads, data managers, statisticians, clinical supplies managers and regulatory ... affairs specialists, etc.. + ensure compliance with relevant regulations,...+ contribute to the development of new drugs and medical devices through clinical trials + May be a… more
- Sanofi Group (Cambridge, MA)
- …and key stakeholders to advance Sanofi's policy objectives. We are an innovative global healthcare company, committed to transforming the lives of people with immune ... recommendations. + Partner with business units, market access, legal, finance, medical , and R&D functions to integrate policy intelligence into product strategy,… more
- IQVIA (Boston, MA)
- …talent for field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more ... As the only global provider of commercial solutions, IQVIA understands what...to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to… more
- IQVIA (Boston, MA)
- …talent for field/inside sales, medical device support, clinical support, and medical affairs our CSMS division has 10,000+ field professionals in more ... Amphastar Pharmaceuticals, Inc. BAQSIMI(R) Job Description As the only global provider of commercial solutions, IQVIA understands what it takes to deliver nationally… more
- Takeda Pharmaceuticals (Boston, MA)
- …of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, ... teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and determined by compliance… more
- Pfizer (Cambridge, MA)
- …(POC) studies in Oncology. You will work in close collaboration with the Global Development Lead (GDL)and members of the development team to establish, lead, ... Medicine, and Digital Medicine). **POSITION RESPONSIBILITIES** + Partner closely with the Global Development Lead (GDL) in the execution of the clinical development… more
- Bristol Myers Squibb (Devens, MA)
- …compilation of Material Review Board (MRB) content for presentation to senior leadership, medical affairs , legal, and other program stakeholders as it relates to ... Therapy manufacturing facility, in accordance with BMS policies, standards, procedures and Global cGMP. They will oversee atypical events to ensure the appropriate… more
- Sanofi Group (Cambridge, MA)
- …ability to partner with colleagues from other functional areas (Market Access & Pricing, Medical Affairs , Commercial). + Agility and flexibility to adapt to ways ... + Develop and maintain collegial relationships with internal cross-functional global /US stakeholders and external alliance partners. **About you** **Experience** :… more
- Takeda Pharmaceuticals (Boston, MA)
- …people to realize their potential through lifechanging work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for ... in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a… more