- Harvard University (Cambridge, MA)
- …& Oper Manager Department Office Location:USA - MA - Cambridge Business Title: Associate Director of Business SupportSub-Unit:Energy & Facilities Salary Grade ... and as a member of a team. + Must project a knowledgeable and professional image to customers and...University. All services are provided in strict accordance with regulatory requirements and customer-determined scopes, with cost recovery almost… more
- Takeda Pharmaceuticals (Boston, MA)
- …excellence and portfolio progression for the Takeda Research pipeline. The AD/ Director of Strategic Outsourcing will provide strategic oversight and relationship ... Takeda Research projects, ensuring alignment with organizational goals, and regulatory and animal welfare requirements. + Cultivate strategic partnerships with… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …plans, scientific reports, briefing packages, clinical study reports, and regulatory labelling interactions. + Provide expertise and guidance on observational ... providers and payers. + Provides input into clinical development, regulatory , reimbursement documents. + Performs/manages, as appropriate, relevant research… more
- Takeda Pharmaceuticals (Boston, MA)
- …to PSPV sub-functions, Documentation & Learning Excellence (DLE), Global Regulatory Affairs (GRA), Global Development Organization (GDO), Clinical Quality (CQA), ... employee onboarding and training activities. + Monitors, interprets, and communicate regulatory requirements and ensure global standards, SOPs, and all associated… more
- Bristol Myers Squibb (Cambridge, MA)
- …literature and deep expertise in neuroscience + Manages cross functional disease project teams with key interfaces in IT, bioinformatics, data sci, stats, external ... Diseases. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …and academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director is typically ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …and/o academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Merck (Boston, MA)
- **Job Description** The Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities ... Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. The Executive Director will manage and oversee the entire cycle of late stage clinical… more
- Humana (Boston, MA)
- …a part of our caring community and help us put health first** The Medical Director relies on medical background and reviews health claims. The Medical Director ... or data requires an in-depth evaluation of variable factors. The Medical Director actively uses their medical background, experience, and judgement to make… more
- Merck (Boston, MA)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director ... and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate… more