- Merck & Co. (North Wales, PA)
- … regulatory administrative activities as needed.Division/AreaResearch and Development Division - Global Regulatory Affairs and Clinical SafetyJob Level/ ... Job DescriptionBrief Description of PositionThe Regulatory Affairs Headquarters Associate Principal Scientist...encompass all aspects of planning and implementation of a global regulatory strategy and regulatory … more
- Merck & Co. (North Wales, PA)
- …corporate standards and policies and business objectives.Actively participate in labeling and global regulatory team meetings to ensure support for anticipated ... Job DescriptionReports to the Director /Senior Director in the Office of...all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to… more
- Merck & Co. (North Wales, PA)
- Job DescriptionPrincipal Scientist / Director , GLOBAL REGULATORY CMC Biologics (R5)Under general supervision of an Executive Director /Senior Director ... Document for projects of increasing complexity.Lead development and execution of detailed, global regulatory submissions of INDs, BLAs or post approval change… more
- Merck & Co. (North Wales, PA)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically, the Director may be… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder the guidance of a Senior Director , within Outcomes Research (OR) the incumbent has the following responsibilities: Development of the integrated ... of patient reported outcomes, epidemiological studies and economic modeling.The Director also works closely with Product Development Teams, Franchise Teams,… more
- Merck & Co. (North Wales, PA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international… more
- Merck & Co. (North Wales, PA)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... Job DescriptionOur company is a global health care leader with a diversified portfolio...of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Director May… more
- Merck & Co. (North Wales, PA)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... Job DescriptionOur company is a global health care leader with a diversified portfolio...and dedicated colleagues while developing and expanding your career.-- Director (Principal Scientist) has primary responsibility for the planning… more
- Merck (Upper Gwynedd, PA)
- **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... advance our pipeline and drive our strategic priorities. The Director , Principal Scientist | Regulatory Affairs...and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical… more
- J&J Family of Companies (Harrisburg, PA)
- …(GRL) - 2406184564W **Description** Johnson & Johnson Innovative Medicine is recruiting for a Director , Global Regulatory Affairs Leader located in New ... Director , Global Regulatory Leader...authority regulated industry + At least 6 years of Regulatory Affairs experience required with focus on the… more
- Merck (North Wales, PA)
- …Description** We are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset ... and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical...external to GRACS. **Key Functions** + Reports to Executive Director or Associate Vice President, General Medicine + Works… more
- Merck (Philadelphia, PA)
- … administrative activities as needed. **Division/Area** Research and Development Division - Global Regulatory Affairs and Clinical Safety **Job Level/ ... **Job Description** **Brief Description of Position** The Regulatory Affairs Headquarters Associate Principal Scientist...Grade** 400 **Reports to** Global Regulatory Liaison, Executive Director … more
- Merck (North Wales, PA)
- …standards and policies and business objectives. Actively participate in labeling and global regulatory team meetings to ensure support for anticipated ... **Job Description** Reports to the Director /Senior Director in the Office of...all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to… more
- CSL Behring (King Of Prussia, PA)
- The Senior Director , Head of Medical Affairs , LatAm & Partner Business will provide strategic, operational, and medical leadership for a high-performance Medical ... of Field Medical organizations are aligned to performance objectives and global Medical Affairs consistent practice. *Ensures responsible clusters' Medical… more
- CSL Behring (King Of Prussia, PA)
- The Senior Director , Global Medical Affairs ...the US and International, Global Market Access, Global Clinical, Global Regulatory , ... Pipeline Hematology is responsible for the development and execution of global medical affairs strategies across the Therapeutic Areas (TA) for pipeline… more
- Kelly Services (Horsham, PA)
- … Affairs Coordinator will help administer the day-to-day Regulatory Affairs operations as directed by the Associate Director related to Product Lifecycle ... Kelly Science and Clinical FSP is currently seeking a Regulatory Affairs Specialist for a long-term engagement...Specialist for a long-term engagement with one of our Global Pharmaceutical clients. This person will join our Kelly… more
- CSL Behring (King Of Prussia, PA)
- The Senior Director Medical Affairs Inline Bleeding will provide strategic medical leadership across all inline bleeding products. This is a critical role to ... key stakeholder to the relevant senior leaders in Medical Affairs in the US and International, Global ...personnel are trained and strong in medical, scientific, and regulatory knowledge as well as industry research and trends.… more
- Organon & Co. (Plymouth Meeting, PA)
- …agile manner. + Provide Regulatory CMC and oversight in developing global Regulatory CMC strategies and executing submissions related to diverse late-stage ... Position** Reporting to the Director or Executive Director in Organon Regulatory CMC New Products,...participating in Agency meetings on CMC topics, and executing global initial marketing applications with a line of sight… more
- Takeda Pharmaceuticals (Harrisburg, PA)
- … Regulatory Project Management and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the ... implementing process changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global … more
- Merck (North Wales, PA)
- **Job Description** **Principal Scientist / Director , GLOBAL REGULATORY CMC Biologics (R5)** Under general supervision of an Executive Director /Senior ... for projects of increasing complexity. + Lead development and execution of detailed, global regulatory submissions of INDs, BLAs or post approval change… more
