- Merck & Co. (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... corporate standards and policies and business objectives.Actively participate in labeling and global regulatory team meetings to ensure support for anticipated… more
- CSL Behring (King Of Prussia, PA)
- …biotherapies used to treat serious and often rare conditions. Could you be our next Associate Director , Global Regulatory Affairs? The job is located ... PA office. This is a hybrid position. You will report to the Director of Global Regulatory Affairs. **Responsibilities:** You are a member of a Regional… more
- Takeda Pharmaceuticals (Exton, PA)
- …to the best of my knowledge. **Job Description** ** Associate Director , US Advertising & Promotion Regulatory Review** **Takeda Pharmaceutical** **Lexington, ... the role:** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review...regulations for development of marketing materials, including representation on global regulatory and labeling teams. + Provide… more
- Merck (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... standards and policies and business objectives. Actively participate in labeling and global regulatory team meetings to ensure support for anticipated… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Global Clinical Quality Date: Jan 7, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job ... risk management activities, and leads continuous improvement for clinical development activities. The Associate Director - Global Clinical Quality leads a… more
- J&J Family of Companies (Spring House, PA)
- We are recruiting for an Associate Director to join the Regulatory Medical Writing team to support the Oncology therapeutic area. The position may be located ... the US; High Wycombe in the UK; or other global locations. Remote work options may also be considered...report directly to the Hematologic Malignancies Disease Area Head, Regulatory Medical Writing, Oncology. + Is the primary point… more
- Merck (West Point, PA)
- …component of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
- Merck (North Wales, PA)
- **Job Description** ** Director Global Marketing** Join our passionate marketing team and be a critical driver in bringing a new oncology asset to customers ... competitive strategy, target product profile development, health authority interactions, global regulatory filing strategy, launch readiness reviews, organized… more
- System One (King Of Prussia, PA)
- …meets industry and regulatory requirements for clinical trial coding. The Associate Medical Coding Director manages and oversees staff, strategic partners, ... Title: Associate Medical Coding Director Full Time...Leads clinical trial coding deliverables and activities that support regulatory commitments including submission of safety data + Provides… more
- Merck (West Point, PA)
- …Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global Clinical Development ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- Merck (Upper Gwynedd, PA)
- **Job Description** **Title: Associate Principal Scientist/ Associate Director , Outcomes Research** **Role Summary** + Under the guidance of a senior leader, ... an Associate Principal Scientist/ Associate Director , has...Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers for use by local subsidiaries in… more
- CSL Behring (King Of Prussia, PA)
- The Associate Director , Corporate Accounts (ADCA) is responsible for optimizing access, reimbursement, and profitability for CSL Behring's portfolio of brands in ... CSL Behring's commercial organization and reports to the Senior Director of Corporate Accounts. The ADCA is responsible for...knowledge of the contracting function and all legal and regulatory requirements. + Proven track record of success to… more
- Publicis Groupe (Philadelphia, PA)
- …| Facebook: www.facebook.com/digitashealth| Twitter: www.twitter.com/digitas_health **Overview** The Associate Medical Director is a medical ... Digitas Health is the Agency of Now: the first global connected-health agency, purpose-built for marketing today. Digitas Health...used in marketing to HCPs. In this capacity, the Associate Medical Director has oversight for the… more
- Merck (West Point, PA)
- …Reporting to the Director of Packaging Commercialization, the Associate Director , Engineering, Packaging Commercialization will lead packaging development ... prior experience developing and commercializing new products on cross-functional teams. The Associate Director will be accountable for the definition and… more
- Wolters Kluwer (Philadelphia, PA)
- . **Marketing Associate Director - Hybrid R0046149** **Job Description** The **Marketing Associate Director ** **,** Segment drives marketing strategy for ... the value of connecting with colleagues. You will report to the Senior Marketing Director and work under the leadership of the VP, Sales and Marketing. This role… more
- Pfizer (Collegeville, PA)
- …clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. + Provide scientifically ... access negotiation, and other evidence generation efforts for Pfizer products; Regulatory and Health Technology Assessment (HTA) submissions; and projects to… more
- Merck (West Point, PA)
- **Job Description** The Global Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company ... Research Laboratories portfolio of clinical trials. Global Clinical Supply is accountable for the planning, sourcing, labeling, packaging and delivery of clinical… more
- Merck (West Point, PA)
- …ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead ... ensure full integration of the device development activities with the clinical, regulatory , formulation, commercial and other key of our company's functions. + Lead… more
- IQVIA (Wayne, PA)
- …problem solving to help clients evolve in a complex and dynamic regulatory environment. **Essential Functions** + Sales role for commercial compliance. + Generate ... significant prospecting and relationship development with senior regulatory and compliance leadership personas. + The role is expected to advance being seen as a… more
- Merck (West Point, PA)
- …relationships with contract manufacturing organizations, + Negotiation of site and global Technical and Quality Agreements, + Participating in contractor GMP audits ... resolution of issues affecting quality and efficiency. + Interpreting complex regulatory requirements for various audiences, including source area management, and… more
