- University of Pennsylvania (Philadelphia, PA)
- …escorting participants to other testing/procedure areas.. . Coordinate several investigational device trials in the cath lab, instruct and support investigators and ... throughout the course of the study. + Creates and maintains research data, regulatory files, subject data and patient tracking databases. + Assures reported trial… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …tools and programs addressing purchasers, payers and policy makers. + Coordinate with Medical & Clinical Affairs , Regulatory to ensure appropriate support ... a minimum of 5-7 years in the pharmaceutical/biotechnology or medical device industry. + In-depth knowledge of...local law. Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Medical Affairs… more
- Envista Holdings Corporation (Quakertown, PA)
- … regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to foster ... Up to 10%, as needed. **PREFERRED QUALIFICATIONS:** + MS degree preferred. + Medical device design and compliance experience. + Compliance Engineering: +… more
- Globus Medical, Inc. (Audubon, PA)
- …technique guides, brochures and other marketing/sales support materials + Partnering with Regulatory Affairs in planning, coordination, writing, and execution of ... role, you must possess the following:** + 8+ years' experience in the medical device product development and research field; 5+ years of people and or program… more
- Wolters Kluwer (Harrisburg, PA)
- …Manager** will be calling primarily on Librarians, Information Scientists, Heads of Global Regulatory Affairs , Directors of Medical Affairs , and ... software tools to for-profit corporations including CROs, pharma and medical device companies. The **Senior Account &...+ Proven track record selling into the pharmaceutical and medical device companies, and CRO's (preferred) +… more
- Envista Holdings Corporation (Quakertown, PA)
- … regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to foster ... Quality Management System (QMS). The position will work together with Regulatory Affairs , Engineering, Operations, and Purchasing/Procurement to ensure product… more
- Cardinal Health (Harrisburg, PA)
- …will also help to support inorganic product opportunities and better define our medical device connectivity strategy. **_Responsibilities_** + Support and be a ... evolution + Collaborate with partners across enterprise, including R&D, Regulatory , Clinical Affairs , Sourcing, Manufacturing, Strategy Functions,...+ 4+ years experience in related field, preferred. + Medical device or global medical … more
- University of Pennsylvania (Philadelphia, PA)
- …involving neuroimaging, blood biomarkers, neuropsychological assessment, and pharmacological and device interventions. TBIRI is seeking a detail-oriented and dynamic ... have prior experience conducting clinical research while adhering to applicable regulatory policies for patient and data protection. Responsibilities include, but… more
- University of Pennsylvania (Philadelphia, PA)
- …Development: Principal support in the development of Physician-Modified Investigational Device Exemptions (PS-IDE) and other clinical protocols for the Division's ... and informed consents documents in collaboration with faculty. + Regulatory -Financial-Training/Continuing Education: Negotiate clinical trial agreements and budgets; conduct… more
- ThermoFisher Scientific (Allentown, PA)
- …+ Minimum 4 years of project management experience in the life sciences, medical device and clinical experience preferred. + Experience developing RUO and ... and customer requirements. + Work closely with R&D, Manufacturing Sciences, Quality, Regulatory , Clinical Affairs and Commercial to define project deliverables.… more