- Astellas Pharma (Westborough, MA)
- …talented counterparts in Quality Control (QC), Cytogenomics, Materials Management, and Regulatory Affairs . This role requires strong leadership, excellent ... ** Manager , Quality Assurance Compliance** Do you want to...related documentation to ensure alignment with internal procedures and regulatory requirements. + Lead, coach, and develop a team… more
- ConvaTec (Lexington, MA)
- …with cross functional team members including, but not limited to, regulatory , R&D, project/ program management, data management, and medical monitors. ... (LSE:CTEC). To learn more please visit http://www.convatecgroup.com **Position Overview:** The Sr. Manager , Clinical Operations plays a key role to the success of… more
- Point32Health (Canton, MA)
- …engagement with senior leaders at contracted provider organizations. + **Risk Adjustment Program Management and Vendor Evaluation** : The Manager will be ... and reporting to identify improvement opportunities and recommend changes to improve program results and effectiveness. The Manager will collaborate with key… more
- Hologic (Marlborough, MA)
- …the highest quality. Collaborate with top talent across Clinical Development, R&D, Regulatory Affairs , Program Management, Legal, Marketing, and Operations ... United States Marlborough, MA, United States Join the Breast and Skeletal Health Clinical Affairs team as a **Clinical Project Manager ,** leading major US and… more
- Eliassen Group (Boston, MA)
- …risk management, and communication across all stakeholders. * Coordinate with Regulatory Affairs to ensure documentation and submission readiness for ... **Project Manager , Med Device, R&D PMO, Design Changes** **Anywhere**...* Partner with cross-functional teams across R&D, Operations, and Regulatory to deliver product design changes that achieve measurable… more
- Beth Israel Lahey Health (Plymouth, MA)
- …conflict resolution + Prior experience in direct responsibility for regulatory affairs and claims management strongly preferred **Registration/Certification:** ... function as a critical element of the system's safety program . As needed, ensures appropriate responses to Adverse Events...disclosure of an event when indicated. + The Risk Manager will lead Root Cause Analyses, Failure Mode Effects… more
- Sumitomo Pharma (Boston, MA)
- …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs , Data Management and Biostatistics is essential. ... support.) + Compile agenda, data, slides, and minutes in collaboration with Program Safety Lead for cross-functional Safety Management Team meetings. + Represent PV… more
- Takeda Pharmaceuticals (Boston, MA)
- …into reality. + Strong understanding of Clinical Trial Delivery and/or Regulatory Affairs /Operations business processes and supporting technology platforms + ... best of my knowledge. **Job Description** **_OBJECTIVES/PURPOSE:_** The Senior Product Manager role involves aligning business and technology stakeholders to develop… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …and biomarker assay development and validation. + Collaborate with Global Manufacturing, Regulatory Affairs , and Global Quality to explore methods and implement ... empower you to shine? Join us as a Senior Manager of Statistics- CMC in our Cambridge, MA office....and/or physical natures and to tailor data analyses to program -specific needs. + Work closely with Takeda statisticians to… more
- AECOM (Chelmsford, MA)
- …of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that ... has an excellent career opportunity for a creative and talented International Development Manager to support implementation of a US Department of State (DOS) funded… more
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