- Globus Medical, Inc. (Audubon, PA)
- …so patients can resume their lives as quickly as possible. **Position Summary:** The Regulatory Affairs Associate assists in drafting, submitting and gaining ... in medical device industry or equivalent, preferably within orthopedic medical devices; Regulatory Affairs experience is a plus. + Excellent communication and… more
- Merck (North Wales, PA)
- …Director/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- J&J Family of Companies (Spring House, PA)
- …& Johnson Innovative Medicine is recruiting for Associate Director, North America Regulatory Lead in Global Regulatory Affairs , supporting programs in ... their potential. At Johnson & Johnson, we all belong. The Associate Director, Regulatory Affairs will be responsible for the development, implementation,… more
- Globus Medical, Inc. (Audubon, PA)
- …faculty members; is available to meet consultant scheduling needs + Collaborates with Regulatory Affairs and Compliance; Reviews and approves all promotional and ... patients can resume their lives as quickly as possible. **Position Summary** **:** The Associate Program Manager, INR is an ideal position for someone who thrives in… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** ** Associate Director, Policy Advocacy** The Associate Director, Policy Advocacy serves as the senior expert in the ... in advancing policy change in support of the company's business objectives. The Associate Director will proactively research and stay abreast of new strategies and… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director of Field Reimbursement is a key role at CSL and member of the US patient experience leadership team. The role is one of two Field ... patient experience, marketing, sales, health care systems, policy advocacy and government affairs (PAGA), medical affairs . + Oversee and champion reimbursement… more
- Merck (North Wales, PA)
- …be able to work with all levels of management within and outside of Global Regulatory Affairs and Clinical Safety (GRACS). + Interact closely with the system ... **Job Description** Under minimal guidance of the Executive Director/Director/ Associate Director, Pharmacovigilance (PV) Partner Strategy & Management (PV-PSM), the… more
- Merck (North Wales, PA)
- **Job Description** **Position Description:** ** Associate Director, Policy Strategy and Capabilities** The Associate Director, Policy Strategy and Capabilities ... team, reporting to the Executive Director, Policy Development & Strategy. The Associate Director will develop and maintain the strategic planning digital platform,… more
- Saint-Gobain (Malvern, PA)
- …to supports its businesses across the US and Canada. Reporting to the Sr. Associate General Counsel of HPS, the Sr. Government Contracts Counsel will have the ... of working with the Saint-Gobain businesses on a multitude of regulatory and Government contract areas and matters. Saint-Gobain businesses, particularly within… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Compliance Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/RA) ... Duties** + Responsible for reviewing of complaint records and performing regulatory reporting assessments of global complaints, preparation and submission of… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be… more