- Chemours (Wilmington, DE)
- …with a primary responsibility for supporting US federal regulatory affairs engagement with the United States Environmental Protection Agency (USEPA), ... time. Chemours is seeking a ** Director of Regulatory Advocacy** to join our growing **Government Affairs...of the political, economic, and social environment in the United States at the federal level. +… more
- CSL Behring (King Of Prussia, PA)
- …GRA functions. + Use global GRA functions to support our goals. Use expertise in US regulatory affairs , coupled with a global perspective, to ensure that ... often rare conditions. Could you be our next Associate Director , Global Regulatory Affairs ? The...Direct regulatory -facing experience + Working knowledge of regulatory guidelines and legislative requirements for US … more
- Merck (West Point, PA)
- **Job Description** **About Us :** The Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular ... utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings. As the AdVAnce facility will not be fully constructed and… more
- Organon & Co. (Plymouth Meeting, PA)
- …are position specific. Please, no phone calls or emails. **Applicable to United States Positions Only:** Under various US state laws, Organon is required to ... **Job Description** **The Position** Reporting to the Director in Organon Regulatory Chemistry, Manufacturing...A better and healthier every day for every woman. ** US and PR Residents Only** For more information about… more
- Takeda Pharmaceuticals (Exton, PA)
- …application is true to the best of my knowledge. **Job Description** **Associate Director , US Advertising & Promotion Regulatory Review** **Takeda ... PA** **About the role:** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory...proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance,… more
- CSL Behring (King Of Prussia, PA)
- …in more than one main region (EU, US , Japan) + Experience in Regulatory Affairs in a global environment across two or more geographic areas **BENEFITS** ... often rare conditions Could you be our next Senior Director , Regulatory Lead-Enabling Healthcare Technologies? The job...an important leadership role as part of the Global Regulatory Affairs (GRA) GPS Leadership Team. You… more
- CSL Behring (King Of Prussia, PA)
- …MA team. + Partner with and share expertise with the _global_ functions of Medical Affairs , ABC, CRD, R&D, Regulatory affairs , Global Clinical Safety & ... Affairs strategies and tactics in support of the US market to demonstrate the value of CSL Behring's...in the assigned TA(s). Provide input on labeling and regulatory strategy. Maintain in-depth understanding of disease states… 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 ... About the role: Join Takeda as a Senior Manager, US Medical Ad/Promo Regulatory Review where you...potential issues. POSITION ACCOUNTABILITIES: + Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance… more
- Organon & Co. (Plymouth Meeting, PA)
- …are position specific. Please, no phone calls or emails. **Applicable to United States Positions Only:** Under various US state laws, Organon is required to ... cross-functional colleagues in preclinical science, data science, clinical operations, regulatory affairs , chemistry, manufacturing and control (CMC), project… more
- Merck (Upper Gwynedd, PA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... regulatory filing, and publication. **Specifically, The Senior Clinical Director May Be Responsible For:** + Evaluating pre-clinical and...in certain states and cities within the United States . Final determinations with respect to… more
- Merck (West Point, PA)
- …with cross-functional teams, including research and development, manufacturing, quality, regulatory affairs , and external partners, to ensure seamless ... **Job Description** The Senior Director of Process Integration and Technology Transfer will...in certain states and cities within the United States . Final determinations with respect to… more
- Pfizer (Collegeville, PA)
- …compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or ... **ROLE SUMMARY** The Medical Digital Health Lead, Sr. Director plays a pivotal role in closing care...any location outside of the United States . Relocation assistance may be available… more
- Pfizer (Collegeville, PA)
- …compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or ... **ROLE SUMMARY** The Director , Global Medical Communications and Content, Oncology will...any location outside of the United States . Relocation assistance may be available… more
- CSL Behring (King Of Prussia, PA)
- …GRA Regional Leadership Team and contributes to the vision and goals for Global Regulatory Affairs (GRA) by: + **Provide leadership to the respective Regional ... and often rare conditions. Could you be our next Director , Advertising and Promotion? This is a hybrid role...years' experience in the pharmaceutical industry, in Biologics/Research & Development/ Regulatory Affairs .** + **At least 7 years… more
- University of Pennsylvania (Kennett Square, PA)
- …high-energy environment. Preference will be given to individuals with experience in regulatory affairs , GLP study directorship, and expertise in animal ... ranks among the top 10 universities in the annual US News & World Report survey. Penn has 12...ecosystem of advanced orthopedic surgery and the translational and regulatory sciences. The Study Director will be… more
- Black & Veatch (Wilmington, DE)
- **Global Benefits Director ** Date: Dec 25, 2024 Location: Overland Park, KS, US US Company: Black & Veatch Family of Companies **Together, we own our ... and perspectives to use. **The Opportunity** The **Global Benefits Director ** will have the opportunity to: + Lead the...risk to the organization. + Ensure compliance with all regulatory requirements + Provide strategic evaluation of our multiple… more
- Merck (West Point, PA)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations). + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- Organon & Co. (Plymouth Meeting, PA)
- …are position specific. Please, no phone calls or emails. **Applicable to United States Positions Only:** Under various US state laws, Organon is required to ... training where needed. + Successfully partner within Global Medical Affairs Capabilities (GMAC), across business functions and geographies to...have proof of legal authority to work in the United States . To apply, create a profile… more
- Army National Guard Units (Gap, PA)
- …or considered for the position. In accordance with section 9902(h) of title 5, United States Code, annuitants reemployed in the Department of Defense shall ... DCSG4 (This includes Combined Support Maintenance Shop - West, Director of Logistics, State Surface Maintenance Office, FMS's 2,...retired under section 8336(d)(1) or 8414(b)(1)(A) of title 5 United States Code) appointed to the Department… more
- University of Pennsylvania (Philadelphia, PA)
- …Ivy League school consistently ranks among the top 10 universities in the annual US News & World Report survey. Penn has 12 highly-regarded schools that provide ... and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will...of the team's work, working closely with the CRU Regulatory coordinators to manage, review and initiate trials to… more