- Merck & Co. (North Wales, PA)
- …corporate standards and policies and business objectives.Actively participate in labeling and global regulatory team meetings to ensure support for anticipated ... Job DescriptionReports to the Director/ Senior Director in the Office of Promotion and...in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed ... drugs for oncology indications. The Associate Vice President will manage and oversee the entire cycle of clinical development, including study design, initiation,… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Ophthalmology will focus on driving strategy, development, and ... excellence in the late development of ophthalmology assets.May serve as a senior therapeutic area content expert within the company, providing input into research… more
- Merck & Co. (North Wales, PA)
- …is based out of Upper Gwynedd, PA, reporting directly to the Associate Director, US Vaccine Portfolio Marketing Strategy & Implementation Lead.- Responsibilities ... Review Team (PRT) approvals, and production.Maintains working knowledge of regulatory guidance & delivers compliant programs.Manages creation and monitoring of… more
- Lilly (Philadelphia, PA)
- …people around the world. **Position Overview:** The Associate Director - CMC Regulatory is responsible for leading global CMC regulatory activities for ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...tools to effectively communicate the status of ongoing CMC regulatory projects to cross-functional teams and senior … more
- Merck (North Wales, PA)
- …standards and policies and business objectives. Actively participate in labeling and global regulatory team meetings to ensure support for anticipated ... **Job Description** Reports to the Director/ Senior Director in the Office of Promotion and...the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval… more
- Takeda Pharmaceuticals (Exton, PA)
- …FDA law and regulations for development of marketing materials, including representation on global regulatory and labeling teams. + Provide leadership related to ... is true to the best of my knowledge. **Job Description** Join Takeda as an Associate Director, US Advertising & Promotion Regulatory Review out of our Lexington,… more
- TE Connectivity (Berwyn, PA)
- Senior Counsel, Global Trade Services -...+ Monitor and keep current on the rapidly evolving global trade environment and trade-related regulatory and ... safer, sustainable and more connected world.** **Job Overview** Global Trade Services (GTS) is a function within the...controls, economic sanctions matters. This role reports to the Associate General Counsel for GTS who heads the GTS… more
- Deloitte (Philadelphia, PA)
- …institution compliance officers, and more. As an Anti-Money Laundering ("AML") Project Associate ( Senior Consultant), you will have the opportunity to help ... please consider an opportunity with Deloitte as a Project Associate . A Project Associate at Deloitte plays...successful client service delivery. The Deloitte & Touche LLP global network includes former bank regulators, federal law enforcement… more
- Merck (North Wales, PA)
- **Job Description** The Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or ... marketed drugs for oncology indications. The Associate Vice President will manage and oversee the entire cycle of clinical development, including study design,… more
- Grant Thornton LLP (Philadelphia, PA)
- As a Real Estate & Construction Advisory Senior Associate , you will have the opportunity to grow and contribute to our global clients' business needs through ... conflicts of interest, organized crime, and other scenarios posing legal or regulatory exposure to our clients + Communicate findings clearly and concisely to… more
- Merck (North Wales, PA)
- **Job Description** The Associate Vice President (AVP)/Section Head, Global Clinical Development, Ophthalmology will focus on driving strategy, development, and ... in the late development of ophthalmology assets. + May serve as a senior therapeutic area content expert within the company, providing input into research and… more
- Publicis Groupe (Philadelphia, PA)
- …department staff + Manage multiple reports at the Director, Manager and Senior Associate level including responsibility for interviewing, hiring, onboarding, and ... Description** Digitas Health is the Agency of Now: the first global connected-health agency, purpose-built for marketing today. Digitas Health specializes in… more
- Merck (Upper Gwynedd, PA)
- …to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical ... **Job Description** The ** Senior Clinical Director (Sr. Principal Scientist)** has primary...closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development… more
- Catalent Pharma Solutions (Philadelphia, PA)
- ** Senior Engineer, Quality Operations** **Position Summary:** Catalent is a global , high-growth, private company and a leading partner for the pharmaceutical ... This 206,878 square-foot facility, located in the Philadelphia area is Catalent's global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP… more
- CSL Behring (King Of Prussia, PA)
- CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious ... CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on...and often rare conditions. Could you be our next Senior Clinical Lab Study Manager? This position is located… more
- ICON Clinical Research (Blue Bell, PA)
- …mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate / Clinical Research Associate II to join ... Senior CRA / CRA II - US -...dynamic team monitoring Hepatology trials. As a Clinical Research Associate , you'll work within a large-scale, fast-paced environment… more
- Merck (West Point, PA)
- …to see if we are the right company for your long-term goals The 2025 Global Supplier Quality Intern, with guidance from the Director/ Associate Director, will ... through the organization, participate on multi-functional teams and interacting with Senior Leaders. The Supplier Quality Management (SQM) organization ensures each… more
- Organon & Co. (Plymouth Meeting, PA)
- …are stored and distributed in accordance with all applicable Organon and regulatory requirements to meet both internal and external customer demands, the Product ... partner and supporting continuous improvement activities. **Primary Activities** + Keeps the Associate Director IMQ Quality (US) informed on the status of operations… more
- Merck (North Wales, PA)
- …is based out of Upper Gwynedd, PA, reporting directly to the Associate Director, US Vaccine Portfolio Marketing Strategy & Implementation Lead. **Responsibilities ... Review Team (PRT) approvals, and production. + Maintains working knowledge of regulatory guidance & delivers compliant programs. + Manages creation and monitoring of… more
