- J&J Family of Companies (Spring House, PA)
- Johnson & Johnson Innovative Medicine is recruiting for a Director , Submission Program Management Leader. This position can be located in Spring House, ... people can reach their potential. At Johnson & Johnson, we all belong. The Director , Submission Program Management Leader (SPML) will be accountable for… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The** **Position** **This position can be 100% remote in the US** The Director , Translational Medicine and Early Development (TMED) Lead will be responsible for ... plans. The TMED Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction with the TMED Operations Lead) and… more
- Pfizer (Collegeville, PA)
- **ROLE SUMMARY** As a member of the Publications Management Team (PMT), the Associate Director , Publications Specialist will be primarily responsible for ... outcomes and create business impact. **ORGANIZATIONAL RELATIONSHIPS** + Reports to Director , Publications Specialist under the Publications Management Sr … more
- System One (King Of Prussia, PA)
- Title: Associate Medical Coding Director Full Time Permanent Opportunity - Direct with the client Onsite King Of Prussia, PA SUMMARY/JOB PURPOSE: The Associate ... Medical Coding Director is responsible for the delivery of timely and...activities. They are responsible for conducting oversight of Data Management Coding activities at the portfolio, as performed by… more
- Compass Group, North America (Wayne, PA)
- …Graves Award for Facility Management Achievement from the International Facilities Management Association (IFMA). Job Summary Senior Director - IFM Solutions ... support teams to assess key bid opportunities and streamline the preparation and submission of successful proposals. + Solutions Process Management : Oversee the… more
- Takeda Pharmaceuticals (Exton, PA)
- …true to the best of my knowledge. **Job Description** **Associate Director , US Advertising & Promotion Regulatory Review** **Takeda Pharmaceutical** **Lexington, MA ... or Exton, PA** **About the role:** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review out of our Lexington, MA or Exton, PA office.… more
- CSL Behring (King Of Prussia, PA)
- …studies accordingly. You will author regulatory dossiers, including briefing documents, submission summary documents (SCE, SCS, CO) and responses to questions. As ... and tactical clinical and medical leadership to assigned clinical development program (s) or individual clinical trial(s) from conceptualization through execution. As… more
- Merck (West Point, PA)
- …process development, qualification, and validation; and design control and risk management techniques to positively support and influence clinical and commercial ... engineering analysis and testing, medical device design controls, risk management , test method/fixture development, design verification and validation, injection… more
- Vanguard (Malvern, PA)
- …Leads and oversees day-to-day monitoring, client due diligence, and client identity management program activities to detect suspicious activity across Vanguard's ... for the development, implementation, and maintenance of compliance processes and program activities. Performs complex compliance sanctions reviews. Serves as a… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Myeloma Research Program Manager (Cancer Center) Job Profile Title Manager Research Project B Job ... Teams that support disease/discipline specific cancer programs within the ACC. This Program Manager will have oversight of the ACC CRU- Myeloma Research Team.… more
- IQVIA (Abington, PA)
- …procedures set forth by IQVIA Biotech and sponsors. Supports the department director in development of functional training, mentoring, and definition of standards ... level compliance with study specific training requirements * Responsible for change management on all assigned projects * Responsible for assuring projects assigned… more
- Takeda Pharmaceuticals (Exton, PA)
- …responsibilities. As part of the US Medical team, you will report to the Director , Ad/Promo Regulatory Review. You will be based in either our Lexington, MA or ... of proposed promotional and disease state materials. + May present to senior management , and present regulatory topics to cross-functional teams. + May serve as… more