- Takeda Pharmaceuticals (Boston, MA)
- …order to bring life-changing therapies to patients worldwide. As an Associate Director , Global Regulatory Affairs Marketed Products you will define, ... and influencing the field as applicable. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple projects.… more
- AbbVie (Cambridge, MA)
- …level will be determined by the qualifications listed below. Purpose: The Associate Scientific Director , Psychiatry Pipeline role provides medical and scientific ... statistics, regulatory , etc) as they relate to on-going medical affairs projects. May assist as consultant/liaison with other corporations when working under… more
- AbbVie (Cambridge, MA)
- …standards, including regulatory guidelines to meet customer needs. Qualifications Associate Scientific Director Qualifications + Bachelor's Degree in the ... level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational… more
- AbbVie (Cambridge, MA)
- …week onsite) in Cambridge, MA preferred. Will consider remote candidates. The Associate Scientific Director provides medical and scientific strategic and ... operational input into core medical affairs activities such as: health care professional and provider...regulatory , etc.) as they relate to on-going medical affairs projects. + May assist as consultant and liaison… more
- Boston University (Boston, MA)
- …Oversight: Lead the central administrative office team and provide supervision to the Senior Associate Director of Residence Life, Associate Director of ... As a pivotal leader within the Division of Student Affairs , the Director of Residence Life reports...Residence Life for Administration, Associate Director of Residence Life for Student & Staff Development,… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …to patients worldwide. Join Takeda as an Associate Director , Global Reg Affairs Device, PDT in our Global Regulatory Affairs CMC & Device ... organization in the Plasma-Derived Therapies Business Unit at Takeda. The Global Regulatory Affairs CMC & Device organization is responsible for global device … more
- Takeda Pharmaceuticals (Lexington, MA)
- …the best of my knowledge. **Job Description** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review out of our Lexington, MA or ... of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and… 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 - GI2 ... TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) on Global Regulatory Teams (GRTs)… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Lead, GI & Inflammation where you ... field as applicable. **How you will contribute:** + The Associate Director will be responsible for complex...regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** ... Here, you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS)… more
- Boston University (Boston, MA)
- …join its team as the IT Audit Manager. This client-facing position reports to the Associate Director , IT Audit & Special Projects, and is responsible for leading ... and constructively with clients, fellow team members, and supervisors; + Lead staff associate or co-sourced IT support resources in the successful completion of IT… more
- Veterans Affairs, Veterans Health Administration (Boston, MA)
- …stress and PTSD. 4. Prepares and ensures compliance with all research regulatory requirements. 5. Prepares and submits initial, ongoing, and final reporting ... research focused committees including editorial boards, grant review panels, and regulatory boards. 1. Academic/Teaching/Training (5% effort) - Will hold a faculty… more
- Veterans Affairs, Veterans Health Administration (Providence, RI)
- Summary This Transportation Assistant position is in the Associate Director 's services at the VA Providence Healthcare Systems, located at the Providence ... promoted to the full performance level without further competition when all regulatory , qualification, and performance requirements are met. Selection at a lower… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …true to the best of my knowledge. **Job Description** **Objectives:** + The Associate Director , Global Scientific Communications, Mature Brands, is a dynamic, ... strategic role within Global Medical Affairs that collaborates with cross-functional partners to own one...Communications planning and execution for mature brands. + The Associate Director , Global Medical Communications is a… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …**Job Description** **About the role:** Reporting into Global Medical Communications, the Associate Director , Global Medical Affairs Congress Excellence Lead ... and manage the annual congress strategic planning process for Global Medical Affairs (including forecasting +3 years) and ensuring proper linkage to the Annual… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Global Medical Communications is a dynamic, strategic role within ... Global Medical Affairs that collaborates with cross-functional partners to oversee one...Medical Communications planning and execution for GI + The Associate Director , Global Medical Communications leads and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , US 3PL Operations Management Lead (Operations & Analytics) **Location** ... : Lexington, MA **About the role:** As an Associate Director of US 3PL Operations Management...Set and maintain all relevant SOPs with Operations, Tax, Regulatory Affairs and Quality + Sustain GDP… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …possible in order to bring life-changing therapies to patients worldwide. As an Associate Director , External Manufacturing & Supply, Cell Therapies, you will ... teams, including analytical development, process development, quality assurance, and regulatory affairs , to ensure seamless project progression +… more
- Takeda Pharmaceuticals (Boston, MA)
- …processes and training and ensure alignment with global processes and regulatory requirements and expectations. + Drive the implementation and change management ... enable execution of CPMQ activities, ensuring alignment with global processes and regulatory requirements. + Create and deliver training solutions to support the… more