- 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
- 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
- Merck (West Point, PA)
- …Us:** The Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late ... 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
- 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
- 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
- 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
- Endo International (Malvern, PA)
- …for talented individuals to join our team. **Job Description Summary** The Associate Director , Commercial Development & Professional Relations will support the ... develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering… more
- Wolters Kluwer (Wilmington, DE)
- . **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
- Merck (West Point, PA)
- …best practices and regulatory compliance. By fulfilling these responsibilities, the Associate Director , Instrumentation and Controls plays a crucial role in ... **Job Description** **Overview:** The Associate Director , Instrumentation and Controls (I&C) plays a pivotal role in ensuring the successful execution of… 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
- CSL Behring (King Of Prussia, PA)
- …the development and management of comprehensive long-term forecasting models for global therapeutic areas, ensuring accuracy and alignment with business objectives. ... on market trends, competitive landscapes, and emerging therapeutic opportunities to inform global forecasting and business strategies * Manage and work with a team… 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)
- **Job Description** Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. The ... and an inspiring mission to achieve new milestones in global healthcare. Our company is on a quest for...seeking a highly motivated candidate for the position of Director , Vaccine Drug Product Development. Vaccine Drug Product Development… more
- CSL Behring (King Of Prussia, PA)
- …of Prussia office. This is a hybrid position. You will report to the Associate Director of Statistical Programming. You will provide hands-on support and ... CSL Behring is a global biotechnology leader, guided by a promise to...will partner with other departments (eg, Biostatistics, Data Management, Regulatory Operations, Medical Writing, ESP teams) to ensure Standard… more
- CSL Plasma (Aston, PA)
- **The Opportunity** The Center Manager reports to the Associate Director Operations (ADO). **The Role** + You will have overall authority for center operations ... business is inspection ready. Meet with QA to include regulatory and customer requirements to ensure the purity and...and employees. Communicate any quality concerns or issues to Associate Director of Operations. + Participate during… more
- Wolters Kluwer (Wilmington, DE)
- …Technology Product Manager - SmartSign Plus** and work under the leadership of the ** Associate Director , Technology Product Management.** This role is a part of ... available - https://www.mywolterskluwerbenefits.com/index.html **Wolters Kluwer (EURONEXT: WKL)** is a global leader in professional information, software solutions, and services… more
- Wolters Kluwer (Wilmington, DE)
- …to experience the value of connecting with colleagues. You will report to the Associate Director , Sales Operations and work under the leadership of the VP, ... available - https://www.mywolterskluwerbenefits.com/index.html Wolters Kluwer (EURONEXT: WKL) is a global leader in professional information, software solutions, and services… more