- Manulife (Boston, MA)
- …team that makes a difference and helps shape the future at Manulife. Senior Director 's key responsibilities include planning, organizing, and assigning audit ... enhance risk control and organizational resilience. We deliver insightful reports to senior management and the Board, reinforcing our commitment to excellence and… more
- IQVIA (Boston, MA)
- …that enable adaptable marketing models to improve patient outcomes. Join us as ** Senior Director ,** **Measurement Product** **Strategy** , and lead one of our ... with data privacy and security standards while navigating complex regulatory landscapes. + Monitor industry trends and emerging technologies… more
- Takeda Pharmaceuticals (Lexington, MA)
- …application is true to the best of my knowledge. **Job Description** Join Takeda as Senior Director - Patient Access Brand Strategy & Operations -Rare Disease BU ... programs, vendor selection and management and performance management. * Partner with senior leadership to ensure strategic initiatives are implemented across Rare. *… 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
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …experts, and the broader scientific community. The role reports directly into the Senior Director , Rare Disease Business Unit Lead. **Job Description** **Key ... **Job Summary** The Director , Medical Communications directs Leads and manages the...company SOPs, GPP (Good Publication Practices), ICMJE guidelines, and global regulatory /legal requirements, establishing governance frameworks to… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …best of my knowledge. **Job Description** **Objectives** + Leads the global Clinical Programs Quality organization, establishing a strategic leadership and oversight ... are resourced, prioritized, and expeditiously reported. + Serves as a senior strategic Quality Partner to relevant R&D stakeholders and strategic suppliers.… more
- Alloy Therapeutics (Waltham, MA)
- …We are Alloy Therapeutics -a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community ... aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. This is an… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …in scientific communication across the portfolio. The position reports to the Senior Director , Nephrology & Immunology Medical Communications Lead and plays ... **Job Summary** The Director , Nephrology & Immunology Publications Lead is responsible...conducted in accordance with internal SOPs, GPP, ICMJE, and regional/ global regulatory requirements + Partner with Legal,… more
- Takeda Pharmaceuticals (Boston, MA)
- …when required. + Provide Clinical Operations leadership under the direction of the Senior Director , Clinical Operations: + Accountable for the overall execution ... activities + Collaborates with and is responsible to the Senior Director , Clinical Operations to ensure adequate...operations approaches to achieving program goals. + Expertise in global regulatory and compliance requirements for clinical… more
- Sanofi Group (Cambridge, MA)
- …that bring hope to patients with some of the highest unmet needs. **The Associate Director , Audit Readiness** will report to the ** Sr . Director , Patient ... CAPA and deviation processes, and ensuring compliance with internal policies, SOPs, and regulatory requirements. The Associate Director will act as the point of… more