- GRAIL (Providence, RI)
- …North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, ... Lab Operations, and other stakeholders to support regulatory strategy development, product validation, audits, promotional material review, on-market product … more
- Parexel (Providence, RI)
- **Job Purpose:** The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... within required timelines + Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage… more
- Daiichi Sankyo, Inc. (Boston, MA)
- …experience in Oncology, clinical research and medical education preferred Principal MSL/ Associate Director MSL5 or More Years' experience including medical ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Olympus Corporation of the Americas (Westborough, MA)
- …problems. The Product Manager may also provide coaching and guidance to Associate Product Managers as required. **Job Duties** + Participate in the ... other marketing activities, under the direction of the Marketing Director or Sr. Product Manager. The ...people's lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare professionals… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial ... processes, ensuring compliance with biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product … more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- **Job Summary** The Associate Director , Global Product Quality - GMP Process is responsible for enabling the optimization and harmonization of key GMP ... continuous improvement. **Key Responsibilities** + Process Ownership & Governance:Lead the global strategy and governance for Product Quality Complaints, CAPA,… more
- Takeda Pharmaceuticals (Boston, MA)
- …the role:** As a Process Scientist ( Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), you will provide technical expertise ... Quality and Global Regulatory Affairs. + SME for Takeda drug product manufacturing organization and network. + In depth and broad understanding of drug … more
- Takeda Pharmaceuticals (Boston, MA)
- …the development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Hematology** proactively ... empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to...in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and… more
- Sanofi Group (Framingham, MA)
- **Job title** : Global Regulatory Affairs Device Lead ( Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** ... and global regulatory authorities to ensure compliance while optimizing product approval pathways. The team is accountable for developing and implementing … more
- Takeda Pharmaceuticals (Boston, MA)
- …and contribute to the company's success. These interfaces include but are not limited to Global Brand Teams (GBTs), Global Product Team (GPTs), Regional and ... leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support… more
- Takeda Pharmaceuticals (Boston, MA)
- …transformative medicines and make a lasting impact on patients worldwide. Join Takeda as Associate Director , Global Regulatory Lead Oncology where you will ... be part of the global regulatory team. As Associate Director...to Lead interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable. + May… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... assigned products in various stages of drug development, which may include one high complexity product and updates to or creation of a new TLP, CCDS, USPI and EU… more
- Takeda Pharmaceuticals (Boston, MA)
- …regulatory strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly ... knowledge. **Job Description** **Objective / Purpose:** + Defines, develops and leads global strategies to maximize global regulatory success towards achievement… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - ... with regulatory strategy for complex programs. + Partner with the GRL to ensure Global Product Team (GPT) regulatory goals are cascaded and that the Global … more
- Publicis Groupe (Boston, MA)
- …is made up of fearless, inventive and generous Unicorns of all kinds. **Overview** ** Associate Director , Digital Product Management - AI Products and ... Gartner, Digitas serves the world's leading brands through a global network comprised of more than 5,500 employees across...Solutions** Digitas is seeking an ** Associate Director , Digital Product Management… more
- Takeda Pharmaceuticals (Boston, MA)
- …grounded in purpose and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Head of Medical Excellence & ... Liaise with members of the GMAO team and key cross-functional stakeholders such as Global Outcomes Research, and be a key contributor to the successful operations of… more
- Sumitomo Pharma (Providence, RI)
- …of ** Associate Director , Regulatory Affairs (Oncology).** The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the ... leads regulatory activities for assigned project(s) in line with the global registration strategy of the product + Supports the global regulatory lead (GRL)… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **Title: Process Engineer Small Molecules API Process Science ( Associate Director )** **Location: Cambridge, MA (Hybrid)** **About the role:** ... As a Process Engineer Small Molecules API Process Science ( Associate Director ), you will provide process engineering support in batch or continuous API platforms… more
- Sanofi Group (Framingham, MA)
- **Job Title:** Associate Director -CMC BioDPDM **Location** : Framingham, MA As Associate Director within CMC BioDPDM, you'll have the opportunity to lead ... could turn the impossible into possible for millions. The Associate Director role is a key leadership...is a key leadership role in CMC Biologics Drug Product Development and Manufacturing. You will be part of… more
- IQVIA (Boston, MA)
- ** Associate Technology Solution Sales Director -eQMS (SmartSolve) & Quality Consulting** The Associate Technology Solution Sales Director will focus on ... with clients to implement **integrated quality strategies** across the product lifecycle, leveraging IQVIA's expertise in regulatory insight, process improvement,… more
