- Veterans Affairs, Veterans Health Administration (Manchester, NH)
- …actively participate in all clinical pharmacy activities as directed by Clinical Pharmacy Program Manager and/or Associate Service Chief - Ambulatory Care. ... as sterile compounding, oncology, controlled substances, medication history review, clinical specialist (anticoagulation, pain, infectious diseases), clinical … more
- Takeda Pharmaceuticals (Lexington, MA)
- …potential issues. **POSITION ACCOUNTABILITIES:** + Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations ... to the best of my knowledge. **Job Description** **Senior Manager , US Medical Ad/Promo Regulatory Review** **Takeda... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- Edwards Lifesciences (Manchester, NH)
- …assigned Regional Director and will collaborate with multiple departments including Sales, Clinical Affairs , Marketing, Quality, Regulatory , and Education. ... around the world. As a part of the Field Clinical Specialist team, you will be a critical part...and support staff trainings. + Collaborating with the Territory Manager on growing the THV therapy through therapy awareness… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Description** About the role Join Takeda as a Medical Grants and Sponsorships Manager where you will develop therapeutic area (TA) medical education strategy and ... you will report to the Sr. Director, US Medical Affairs . This is a hybrid position based in Lexington,...well as Global functional groups such as Medical and Clinical Development. + Liaise with external key stakeholders such… more
- Takeda Pharmaceuticals (Concord, NH)
- …relationships among functions represented at the Labeling cross functional teams including clinical , safety, medical affairs , device regulatory and ... therapies to patients worldwide. Join Takeda as the Senior Manager , Global Labeling Devices. You will be responsible for...as the expert for device labeling on the global Regulatory Affairs (RA) Sub team and Global… more
- Edwards Lifesciences (Concord, NH)
- …our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for ... clinical trials with skill levels exceeding the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead +… more
- Fujifilm (Concord, NH)
- …+ Proven track record working with Marketing, Business Development, Engineering/QA, and Regulatory Affairs . + Competitive knowledge of Medical IT and Imaging ... US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all...at least 1-2 years direct experience as a Product Manager within HCUS/MIPD + Strong understanding of clinical… more
- AbbVie (Waltham, MA)
- …(Biomarker research, Regulatory , Pathology, Clinical Science, Biosample Management, Clinical Operations and Medical Affairs ) + Manage activities and tech ... a highly motivated individual to join our Precision Medicine team as a Manager , Companion Diagnostics Operations. The CDx Operations Manager will work closely… more
- ConvaTec (Lexington, MA)
- …project work + **Scientific & Technical Labs** to execute testing, as required. + ** Regulatory Affairs ** to collaborate on requirements as well as gain early ... the form of technical presentations & reports. + Collaborate with project management, regulatory , clinical , etc. teams to stay aligned on key goals,… more