- Merck & Co. (North Wales, PA)
- …the 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
- 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 ... Job DescriptionThe Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed… more
- 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
- Takeda Pharmaceuticals (Exton, PA)
- …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... of my knowledge. **Job Description** Join Takeda as an Associate Director, US Advertising & Promotion Regulatory ... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …Regulatory Project Management and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global ... changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global Regulatory Project Management… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …FDA/EMA/PMDA regulations; ICH guidance; GLP/GCP requirements; SEND requirements, etc.). + Regulatory Affairs Credential (RAC-Drugs) is an advantage. + Strong ... to the best of my knowledge. **Job Description** **About the role:** ** Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology… more
- University of Pennsylvania (Philadelphia, PA)
- …resources, and much more. Posted Job Title Quality Assurance Specialist ( Regulatory ) CVPF(Center for Cellular Immunotherapy) Job Profile Title Research Coordinator ... to help with raw materials release, new hire QA Associate train. Position contingent upon funding. Qualifications + Bachelor...allows you to relax, take vacations, attend to personal affairs , recover from illness or injury, spend time with… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director, Medical Excellence and Impact - 2406214789W **Description** Johnson and Johnson Family is recruiting an ** Associate Director, Medical** ... of the disease. **Position Overview:** We are seeking a dynamic and forward-thinking Associate Director, Medical Excellence Lead to join our team. This role is… more
- J&J Family of Companies (Horsham, PA)
- Associate Director, MSL Communications - Immunology - 2406205683W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate Director, ... impact health for humanity. Learn more at https://www.jnj.com/ . The Associate Director, Medical Science Liaison (MSL) Communications, will be responsible for… more
- J&J Family of Companies (Horsham, PA)
- Associate Director, Real World Value and Evidence - Hematology - 2406214039W **Description** Johnson & Johnson is currently recruiting an Associate Director, ... humanity. Learn more at https://www.jnj.com/. In this in-house position, the Associate Director, RWV&E, will be responsible for conducting real-world evidence… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be responsible for the ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… 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
- J&J Family of Companies (Horsham, PA)
- …experience. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs , Clinical, Medical Information, Pharmacovigilance) including at ... Associate Director, RA Labeling Product Leader (1 of...least 6 years of direct regulatory labeling content experience developing and writing labeling content… 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
- J&J Family of Companies (Horsham, PA)
- …collaborating and communicating cross-functionally with competitive intelligence, finance, medical affairs , regulatory and other key functions + Present ... Associate Director, Global Commercial Insights and Analytics, Autoantibody...- 2406206641W **Description** Johnson & Johnson is seeking a Associate Director, Global Commercial Insights and Analytics, Autoantibody to… 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
- University of Pennsylvania (Philadelphia, PA)
- …Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work closely ... of the team's work, working closely with the CRU Regulatory coordinators to manage, review and initiate trials to...+ The candidate will work closely with the CRU Associate Director of Operations to develop and implement SOP's,… more
- Elevance Health (Wilmington, DE)
- …and tactical issues. + Work collaboratively with other teams, including legal, compliance, regulatory affairs , in supporting the business. + In a complex and ... ** Associate General Counsel Sr. - Pharmacy** **Location:** This...infusion and specialty Pharmacies, strategy, licensing, compliance, innovation and regulatory matters. As such, this position requires a keen… more
- J&J Family of Companies (Titusville, NJ)
- …. The Manager, Medical Information Scientific Engagement (MISE) reports to the Associate Director MISE and is responsible for engaging healthcare professionals (HCP) ... requests for information from internal and external customers consistent with regulatory guidelines. * Documents interactions in Customer Relation Management (CRM)… more
