- 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 ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… 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
- Merck (Trenton, NJ)
- …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
- Bristol Myers Squibb (Trenton, NJ)
- …lives. Read more: careers.bms.com/working-with-us **Position Summary** The Associate Director , Long Range Supply and Capacity Planning Global Process ... work and in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** ** Associate Director Long-Range Supply and Capacity Planning - GPL**… more
- J&J Family of Companies (Trenton, NJ)
- Associate Director , Clinical Trial Learning & Training - 2406187889W **Description** Johnson & Johnson is recruiting for an ** Associate Director , ... profoundly impact health for humanity. Learn more at https://www.jnj.com/ . The Associate Director is responsible for deploying organizational training strategy… more
- Wolters Kluwer (Trenton, NJ)
- …here. (https://youtu.be/OZ2kSzAaXK4?si=sDgZ7DZUbMnBddMq)** **What We Offer: ** The Market Research Associate Director role offers growth potential opportunities, ... Wolters Kluwer is a global leader in professional information services that combines...benefits. **What You'll be Doing:** As our Market Research Associate Director , you will share your in-depth… more
- Merck (Trenton, NJ)
- …(QCI) colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) ... the global inspection tracking system that tracks all GCP Regulatory Health Authority inspections, findings, responses and Corrective Action and Preventive… more
- Merck (Trenton, NJ)
- …Medical Device and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible ... reviewing and approving medical device/combination product documentation to support regulatory filings and audits of data, policies, procedures, and systems… more
- Novo Nordisk (Plainsboro, NJ)
- About the Department The Clinical Development, 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 (Trenton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Portfolio Management Insights, Portfolio & Strategic ... (P&SO), drives portfolio management insights development and delivery to the Global Program Teams (GPTs), Therapeutics Areas (TAs) leaders, Hematology Oncology Cell… more
- Bristol Myers Squibb (Trenton, NJ)
- …the opportunity to leverage the best-in-class oncology capabilities of BMS. The Associate Director , Program Management will be accountable for the ... managing clinical development teams and successfully advancing development candidates to global regulatory submissions (INDs/CTAs) * Ability to execute diverse… more
- Zimmer Biomet (Mount Laurel, NJ)
- …included, respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to ... of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a...- Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio… more
- Bristol Myers Squibb (Trenton, NJ)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing ... of Medical Strategies, Objectives and FM Plans within boundaries established by regulatory and legal compliance in accordance with company policies and sound ethical… more
- Bristol Myers Squibb (Trenton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Supplier Risk and TPRM role will support BMS' Supply ... **Risk & TPRM Strategy and Process** + Support in the execution of the global supply chain risk management strategy that is aligned with the company's objectives and… more
- Integra LifeSciences (Plainsboro, NJ)
- …are challenging what's possible and making headway to help improve outcomes. The Associate Director , Instruments & Lighting Marketing role will have end-to-end ... including field sales, country marketing teams, product development, finance, regulatory , clinical/medical affairs, business development and others; demonstrates strong… more
- Novo Nordisk (Plainsboro, NJ)
- …Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent, ... focusing on optimizing patient care and support. Relationships Reports to the Director of PSP Analytics and Ops Excellence. Key internal relationships include… more
- TD Bank (Mount Laurel, NJ)
- …this role. **Line of Business:** Risk Management **Job Description:** The Regulatory Relationship Associate provides strategic oversight, assistance, and ... on Internal Audit responses. + Support audit teams for regulatory matters. + Contribute to Board of Director...We Are:** TD is one of the world's leading global financial institutions and is the fifth largest bank… more
- Marriott (Trenton, NJ)
- …with the Global Information Security team and ensure that all regulatory standards and followed and implemented. The leader also set up governance, policy, ... **Position Type** Management **JOB SUMMARY** Marriott International (MI) is transforming its global network technology to offer the most advanced, most secure, most… more
- Merck (Trenton, NJ)
- … Director ) as needed. + Works in partnership with GCTO ( Global Clinical Trial Operations) country operations, finance, regulatory affairs, pharmacovigilance, ... **Job Description** With support of Sr CRA (Clinical Research Associate ) and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a… more
- Church & Dwight Co., Inc. (Ewing, NJ)
- …of Vegetarian NPD and non-GMO offerings. This role will work closely with the Associate Director to refine these strategies and execute with urgency and ... (Gravol, Rub A535), general responsibilities will also include: Strategy: + Support the Associate Director in the development, execution and tracking of growth… more