- Staffing Now (Philadelphia, PA)
- …to building type. Ensures buildings are managed in accordance with all regulatory requirements.* Manage leasing and annual/interim recertification process in ... Clerks, Receptionists, and internal and contracted Custodians.* Directly supervise in Director 's absence or provide support to Property Managers throughout the… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project Management and Strategic ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information... Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project… more
- Ascendis Pharma (Princeton, NJ)
- The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for labeling activities across programs and stages of development, with specific ... for regulatory submissions and product maintenance. The Associate Director prioritizes their own work to...external partners may be required. Key responsibilities: . Drive process for development and management of US & Americas… more
- Novo Nordisk (Princeton, NJ)
- …lives for a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide ... positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion....to maintain efficient and compliant Promotional Review Board (PRB) process + Serve as a primary regulatory … more
- Merck (North Wales, PA)
- …solutions to the world. **Looking for someone with a growth mindset. The Director , Regulatory Affairs Liaison is responsible for:** + Developing regulatory ... **Job Description** Our Regulatory Affairs team bring new medical advancements to...but are not limited to:** + Reports to Executive Director or Associate Vice President, Therapeutic Area… more
- Novo Nordisk (Princeton, NJ)
- …clinical development and regulatory requirements of a clinical program. The Associate Director will provide high level strategic input into development ... plans, study designs, and regulatory submissions. Relationships The Associate Director...+ Demonstrated understanding of clinical research, the drug/device development process , and applicable regulatory guidelines + Demonstrated… more
- Amicus Therapeutics (Princeton, NJ)
- …with Technical Operations, Regulatory and other internal partners, the EQL Associate Director is actively engaged in ensuring outsourced manufacturing is ... existing products and Continued Process Verification (CPV) activities. The EQL Associate Director will work to build and maintain effective relationships… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , Statistical Programming , provide s functional expertise ... implementation of technical solutions for integrating, analyzing and reporting clinical data. Associate Director d rives the development and implementation of… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Clinical Pharmacology and Pharmacometrics - 2306103445W **Description** Janssen Research & Development, LLC is recruiting for an Associate ... abreast of clinical pharmacology, MIDD, analysis methodology and overall drug development process , including regulatory guidance, and methods in modeling and… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Clinical Pharmacology and Pharmacometrics - 2406183146W **Description** Johnson & Johnson Innovative Medicine is recruiting for an ... Associate Director , Clinical Pharmacology and Pharmacometrics, located...for the development of a compound, including interactions with regulatory agencies and functions as CPP Leader on the… more
- Merck (West Point, PA)
- … regulatory requirements, regulatory filings and company policies. The Associate Director also ensures that effective and robust Quality systems are ... **Job Description** The Associate Director , ESQL is responsible for...EQA and Division in specific Quality systems, technology platforms, regulatory expectations and/or EE management, and can represent the… more
- Bristol Myers Squibb (Trenton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Clinical Nurse Consultant** _The Clinical Nurse Consultant ... (CNC) Associate Director is the leader of a...and dependability + Current working knowledge of US legal, regulatory , and compliance regulations and guidelines + Excellent computer… more
- Merck (West Point, PA)
- … Process Development, Commercialization, Operations, Technical Operations, Analytical, Quality, Regulatory -CMC, and Supply Chain. Associate Director is ... **Job Description** **Position Description:** ** Associate Director ,** **Technology Transfer** **(TT)** **Systems...+ Required to comply with our company Global and regulatory requirements and execute current Good manufacturing Practices (cGMP)… more
- Merck (Trenton, NJ)
- …component of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an...Associate Director will work with scientists within… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Title:** Associate Director of Consumer Marketing We are seeking an experienced, ... passionate and results-driven Associate Director of Consumer Marketing to help support the consumer marketing efforts focused on schizophrenia. The Associate … more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Scientific Patient Engagement Research - 2406186600W **Description** Johnson and Johnson is recruiting an Associate Director , ... for humanity. Learn more at https://www.jnj.com/. The Scientific Patient Engagement Research Associate Director is responsible for leading and driving high… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Sciences Pleasanton, CA, USA * Princeton, NJ, USA Req #361 Monday, April 22, 2024 Looking for a chance to make a meaningful difference in ... on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the...limited to- safety reporting, query resolution, SAE reconciliation, un-blinding process , and safety reporting training. + Participate in the… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible for the ... By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application… more
- Novo Nordisk (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Scientific Associate Director , DMPK Project Representative** Challenging. Meaningful. ... across the globe. PCO is looking for a Scientific Associate Director to join the Dev DMPK...activities of multiple projects; be responsible for preparation of regulatory dossier/responses; and assist in developing strategy for the… more
