- Medtronic (Boston, MA)
- …guidance you need to own your future success. Together, we can transform healthcare. The Senior Director of Regulatory Affairs will lead the Regulatory ... technologies to market. It involves creating, managing and executing global regulatory strategies for new product development... staff and coach to ensure continuing development of regulatory skills + Keep Senior Management informed… more
- AbbVie (Boston, MA)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director , Global Regulatory Lead, is responsible for developing and ... maintain market approval for product(s) in the assigned therapeutic area. Leads the Global Regulatory Product Team (GRPT). Continually expands TA knowledge, and… more
- Sanofi Group (Cambridge, MA)
- …advertising and promotion of prescription drugs and biologics. Essential Functions + Represents Global Regulatory Affairs (US RA AdPromo) as a member of ... About the Role The Associate Director , US Regulatory Affairs (RA) serves...and long-term business objectives while mitigating risk. Consults with senior management and provides input to the global… more
- Manulife (Boston, MA)
- …Arrangement** Hybrid **Job Description** **Institutional Client Platform Product Manager, Senior Director , Global Institutional, Manulife Investment ... Management** **Job Title** : Senior Director , Global Institutional Client Platform The Institutional Client Platform Product Manager will report to the … more
- Takeda Pharmaceuticals (Boston, MA)
- …oncology opportunities for either partnering and/or investment. + In collaboration with Global Regulatory Affairs (GRA), monitor and communication with Takeda ... empowered to achieve your best. As part of the Global Oncology Products and Pipeline Strategy team, you will...Identify, monitor and review near-term (within 3 years of regulatory approval) oncology partnering opportunities + Lead / co-lead… more
- Sanofi Group (Cambridge, MA)
- …+ Leads the US regulatory activities. + As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global Regulatory ... expertise to contribute to the definition of the global regulatory strategy, to enable and drive...regions / GRA-CMC /GRA-Devices to communicate the outcome to senior management as needed + May lead Health Authority… more
- Sanofi Group (Cambridge, MA)
- …Leads the US regulatory post-marketing activities. + As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global ... expertise to contribute to the definition of the global regulatory strategy, to enable and drive...regions / GRA-CMC /GRA-Devices to communicate the outcome to senior management as needed + May lead Health Authority… more
- Sanofi Group (Cambridge, MA)
- …in regulatory policy efforts. Reporting through Region North America within Global Regulatory Affairs (GRA), the candidate will work collaboratively with ... to have a positive impact on the environment advise internal stakeholders on evolving regulatory policy issues, and more! The Director will be a strong subject… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …clinical drug discovery and development + TMS state-of-the-art technologies + Regional/ global Regulatory requirements + GCP/ICH **Takeda Compensation and ... is true to the best of my knowledge. **Job Description** **Job Description for Senior Medical Director , Clinical Science, Marketed Products Development** As the … more
- Merck (Boston, MA)
- …placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be responsible for:** + Providing scientific ... mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with...all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle… more
- Takeda Pharmaceuticals (Boston, MA)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Director , GRA Pharmaceuticals- Small Molecule where you will establish ... Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs -...regulatory team in the development and implementation of global CMC regulatory strategies during development ,commercialization… more
- Bristol Myers Squibb (Cambridge, MA)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Director will be the clinical lead to progress multiple early ... Area Description** The Early Clinical Development function is part of a global scientific organization dedicated to initial evaluations of new molecules, biomarkers,… more
- Bristol Myers Squibb (Cambridge, MA)
- …and make a difference. As part of the Discovery Biotherapeutics efforts at BMS, the Senior Director of Protein Engineering will play a key role in discovering ... and delivering a first-in-class and best-in-class Biotherapeutics pipeline. The Senior Director , Protein Engineering, will be responsible for leading a team of… more
- Editas Medicine (Cambridge, MA)
- …more equitable future. Position Summary Reporting to the VP of Biometrics, the Director /Sr. Director , Clinical Data Management is responsible for all clinical ... processes, and excellent people leadership skills. Key Responsibilities: + As the Director /Sr. Director , Clinical Data Management, you will be responsible for:… more
- Regeneron Pharmaceuticals (Boston, MA)
- …Nervous System, Peripheral Nervous System, Neuromuscular and Muscular Diseases. **As a Senior Medical Director , a typical day may include the following:** ... functions + Contributes to overall Program strategy and interacts with Regulatory , Clinical Pharmacology, Research, Non Clinical functions, and more, to create… more
- Merck (Boston, MA)
- …the Associate Vice President in Vaccine/Infectious Disease (VID), Epidemiology, the Senior Director , Epidemiology has lead management and oversight ... by the therapeutic area (TA) Associate Vice President. + Reviews regulatory documents, reports, and publications within assigned products or indications in… more
- Bristol Myers Squibb (Cambridge, MA)
- …The Clinical Development Lead sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. ... with target label indications and are designed to meet regulatory , quality, medical, and access goals + Serves as...a given Target Product Profile (TPP) + Collaborates with Global Development Operations/ Global Compliance Group to develop… more
- RELX INC (Cambridge, MA)
- …training approach and drive execution of a best-in-class sales training program worldwide. The Director of Global Sales Performance will be a global sales ... LexisNexis Legal & Professional(R), a part of RELX, provides legal, regulatory , and business information and analytics that help customers increase their… more
- Sanofi Group (Cambridge, MA)
- The Senior Clinical Research Director (Sr CRD)...Interact with other CRDs in the project, Principal CRD, Global Project Head, The PV Rep, Regulatory ... analytical skills and the ability deliver to multiple operational tasks. The role of the Senior CRD is to: + Act as a mentor for other CRDs and Clinical Scientists… more
- Marriott (Boston, MA)
- **Additional Information** Senior Director - Growth Initiatives **Job Number** 24077908 **Job Category** Information Technology **Location** Marriott ... and other key performance metrics + Supports Sarbanes-Oxley, ISP, and other regulatory compliance matters with service providers + Monitors and supports following… more