- Hologic (Marlborough, MA)
- …of our San Diego or Marlborough campus, and are looking for a Regulatory Affairs Manager , responsible for on-market regulatory activities associated with US FDA, ... Manager , Regulatory Affairs (IVD On-Market/Sustaining) San...vitro diagnostic systems, including software and hardware; to meet project timelines and / or regulatory obligations. + Work… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, quality assurance, etc.) in pharmaceutical or ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed. Works… more
- Medtronic (Mansfield, MA)
- …Manage multiple projects and prioritize tasks on day by day basis to meet project schedules + Interface with engineering, quality, clinical , marketing, and other ... in the Life** We are seeking a Senior Regulatory Affairs Specialist to join our team within Medtronic Acute...global compliance. You will collaborate closely with engineering, marketing, clinical , quality as well as the regional and international… more
- Takeda Pharmaceuticals (Boston, MA)
- …execution of medical strategies by the US medical team and partner with the project manager (PM) to track progress against strategic plans, including the ... your best. As part of the US Oncology Medical Affairs team, you will report to the Scientific Director...+ Tactical accountability grounded in science, disease state, competitive clinical data in support of one or more products.… more
- ConvaTec (Lexington, MA)
- …Portfolio Management team for Medical and Clinical Affairs , the Clinical Program Manager oversees the project management, planning, execution, ... us on our journey to #ForeverCaring as a Senior Clinical Program Manager , and you won't either....**Principal Contacts & Purpose of Contact** MACA (Medical and Clinical Affairs ) organization to exchange information and… more
- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of **Senior Manager , Clinical Supply Chain** . The Senior Manager , ... programs. In addition, working closely with CMC, Regulatory Affairs , Quality Assurance, Clinical Operations, and /or...Knowledge of Interactive Response Technology (IRT) systems used in clinical studies. + Excellent project management and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Operations, Regulatory, CMC, Marketing). + Minimum of 5 years' experience as a clinical project /program manager leading complex pharmaceutical, academic or ... Evidence Generation, US Medical** **Lexington, MA** **Hybrid** **_OBJECTIVES/PURPOSE:_** Provides clinical project management and leadership to ensure successful… more
- Takeda Pharmaceuticals (Boston, MA)
- …with customers and accounts via partnership with field representations (Key Accounts, Clinical Sales, Medical, etc.) Extend the impact of IBD Leadership efforts to ... vendors ensuring internal stakeholder alignment across agency partners, PRT, medical affairs , compliance and IT. **Thought Leader Engagement:** Identify, build and… more
- Beth Israel Lahey Health (Burlington, MA)
- …education activities and attends conferences/seminars to maintain current knowledge of clinical study affairs and issues.** **Participates and assists in ... a difference in people's lives.** Under general direction, the Research Program Manager will be responsible for managing, promoting, cultivating and overseeing all… more
- Fujifilm (Boston, MA)
- …for the Fujifilm Healthcare Americas Corporation IT portfolio. The Global Product Manager (GPM) is responsible for developing product plans, acting as a Product ... meet the plan's objectives. The GPM reports to the Manager , Product Planning and is able to fill in...but are not limited to: + Creation of: + Project Charters. + Market Requirements Definition (MRD). + Product… more
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