- Merck & Co. (Rahway, NJ)
- …of carefully designed clinical trials is critical to drug development.The Associate Director , Clinical Trials Communications role within our Research ... clinical trials among diverse populations through communications strategies.Support priority clinical trial programs across the portfolio with customized… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. Job Summary The Associate Director , Clinical Outsourcing, will oversee and lead and support activities ... development.#LI-TS1Eisai Salary Transparency Language:The base salary range for the Associate Director , Clinical Outsourcing is from :157,200-206,300Under… more
- George Washington University (Washington, DC)
- …The George Washington University (GW) is actively seeking a dedicated and experienced Associate Director , Clinical Services to join the leadership team ... model and short-term counseling framework, thus guaranteeing superior, personalized care.Beyond direct clinical duties, the Associate Director is tasked with… more
- George Washington University (Washington, DC)
- …faculty and the Field Work Coordinator, the Associate Director of Clinical Education Programs partners on program design, development, clinical ... Director of Clinical Education... programs . Coordinate and schedule orientation and clinical education compliance activities. Organize Program meetings… more
- Merck & Co. (North Wales, PA)
- …of clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct/indirect team members ... drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program... clinical studies. Under the direction of the Program Lead, you will collaborate with global, cross-functional team… more
- Compass Health Network (Windsor, MO)
- The Associate Director of Clinical Services assists the Vice President of Clinical Services with administrative and clinical operation of the ... in the provision of psychology services. Responsibilities of the Associate Director of Clinical Services:...supplies and facility costsAssist with establishing a quality assurance program , in conjunction with the CQI team, which implements… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team ... cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo... to lead our in vivo CAR-T cell therapy program . If you're passionate about advancing groundbreaking treatments and… more
- Catalent (Manassas, VA)
- Associate Director , Regulatory Affairs Position Summary: Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry ... consumer and Catalent employee. The primary duty of the Associate Director , Regulatory Affairs is to support...(including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence,… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at ouor 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 QP2 by applying...minimal supervision and/or lead QP2 efforts on drug/vaccine development programs , and author or co-author strategic documents. Associate … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction ... of the Senior Director , GMA Oncology (Global Medical Affairs team lead for...lead for compound), is responsible for assisting with defining compound/ program medical strategies and for leading select medical affairs… more
- Merck & Co. (North Wales, PA)
- …lead development of and maintain publication strategy and plans in the assigned oncology program . The Associate Director Pub Manager delivers the tactics ... Job DescriptionOverview:The Associate Director Publication (Pub) Manager is...for stakeholders as needed.Build and maintain excellent relationships with clinical investigators, scientific leaders, external authors, journal editors, and… more
- Merck & Co. (Rahway, NJ)
- …and/or medical device industries to set tactical and strategic direction on programs they lead to ensure high quality products and robust manufacturing processes.-- ... and risk management techniques to positively support and influence clinical and commercial combination product development and launches.Principal ResponsibilitiesLead… more
- Novo Nordisk Inc. (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 ... ready to make a difference? The Position The Assoc Director OED - Supplies, is responsible for US and...This includes leading processes and technology improvements to link Clinical trial site needs, Finance and Supply forecasts that… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and...data acquisition, processing, and reporting of external data across programs . Monitor vendor performance by collection and review of… more
- Novo Nordisk Inc. (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 ... processes (ie automation, technology, process optimization). Relationships Reports to Director or above within CMR Training & Knowledge Management. Collaborates… more
- Insmed Incorporated (Bridgewater, NJ)
- …organizations etc.) to build and to execute the bioanalytical strategy specific to clinical development programs .Participate in clinical study design and ... for Millennials™ lists.OverviewWithin the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …& independently in order to accomplish objectives. Relationships Reports to the Director , Patient Support Programs Rare Disease. Key internal relationships ... the day-to-day operations of the Rare Disease patient access and support programs . Additionally, this person will be responsible for driving new initiatives related… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …analysis dataset specifications and ensure correct interpretation of SAP, develop independent programs to validate stud level analysis dataset and TLFs generated by ... to support submission QAs, perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory Committee Meeting-… more
- Catalent (Harman, WV)
- Senior Director , Supply Chain Position Summary: The Senior Director , Supply Chain is responsible for leading the supply chain organization for Catalent Maryland. ... coming online.Reporting to the Vice President and General Manager, the Senior Director Supply Chain directs all facets of supply chain management including, but… more
