- Merck & Co. (North Wales, PA)
- … trials and will interact externally with key opinion leaders.Specifically, the Associate Vice President may be responsible for:Evaluating pre- clinical and ... Job DescriptionThe Associate Vice President (AVP) has primary responsibility for...(AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs for… 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 ... into research and business development priorities and prioritization of clinical assets.-May serve as the senior liaison...to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... Clinical Pharmacology and Modeling & Simulation plans from FIH...high-level supervision; participates in due diligence activities and represents global function on study and project teamsProduces independent writing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... position, task oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence to Project objectives,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... safety monitoring and risk management activities, provides insights on current clinical practice and guidelines, reviews and provides written assessments of relevant… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... team and serves as ad hoc member to the Global Project Team for late stage projects. This position...technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …decision-makers across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions ... About the Department Our East Coast Global Development Hub brings together the best minds...NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating… more
- Aequor (Thousand Oaks, CA)
- …products and biosimilars. DSC arranges and ensures the product needed for 's clinical trials is available globally. DSC serve patients around the globe and ensure ... the patients to receive their dose on time. The Global Study Planning (GSP) team is responsible for forecasting...to patient every time. During the length of the clinical trial, the study planner is responsible to monitor… more
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director/ Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... standards and policies and business objectives.Actively participate in labeling and global regulatory team meetings to ensure support for anticipated promotional… more
- Merck & Co. (Rahway, NJ)
- …Dosage (Non-Sterile) team at the FLEx Center in Rahway is looking for an Associate Director - Process Engineer to lead clinical supply manufacturing, scientific ... is a multi-modality (small molecule, biologics, vaccine) Drug Product development and clinical manufacturing facility in Rahway, New Jersey.- This team works with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Effectively uses and communicates key findings and presents recommendations to Senior Regional and Global Finance Leaders.- Annual Portfolio Prioritization ... people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...and is accountable for the development and control of Clinical Project Budget in support of Phase I-III … more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & Division organization of ... our company.- Position Description/Summary: The GPAM Associate Director, Project Manager, is a core member of Early Drug Development and/or Late Drug Development… more
- Aequor (Thousand Oaks, CA)
- …consistent basis. Job Details: Under minimal supervision, manage demand and supply of Pre- Clinical and Phase I Clinical Programs. The position requires project ... Responsibilities will include gathering demand requirements and driving production of Pre- Clinical and Clinical Investigational products, as well as tracking… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …within responsible therapeutic / franchise area(s). Relationships Reports to Senior Director, Value Communication and Contracting Strategy. Interacts frequently in ... collaboration with internal management and senior level managed markets customer representatives. Interacts internally with team representatives from Finance,… more
- Tris Pharma (Monmouth Junction, NJ)
- …have an immediate opening in our Monmouth Junction, NJ facility for an Associate Director, Alliance Management.Tris Pharma has a long track record of successful ... alliances, from global commercial partnerships to R&D collaborations to manufacturing/distribution partnerships....departments across all stages of the product lifecycle. The Associate Director, Alliance Management will be accountable for managing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the safety surveillance sub-function within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and Senior ... professionals, HAs, ECs, DMCs, and Academia. Line management of Senior Global Safety Lead(s), Global ... Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential… more
- Merck & Co. (Rahway, NJ)
- …Biologics and Biopharmaceutics, have 8-10 direct reports composed of experienced, senior and associate biopharmaceutic scientists.- The successful candidate will ... Job DescriptionOur company is a global health care leader with a diversified portfolio...across organizations such as Regulatory CMC, formulation functions, and clinical functions to ensure timebound progression of portfolio, initiatives… more
- Xenon Pharmaceuticals Inc. (Boston, MA)
- …development, corporate, and commercial operations. About the Role: We are seeking a Senior Manager/ Associate Director, Supply Chain Planning to join our team. ... The Senior Manager/ Associate Director, Supply Chain Planning will...small molecule drug development programs in support of Xenon's clinical trials. The Senior Manager, Supply Chain… more
- Rakuten Medical Inc. - US (San Diego, CA)
- Position Summary Reporting to the Chief Technology Officer, the Senior Manager/ Associate Director of Clinical GCP Quality will be responsible for evaluating ... and mitigating risk of global clinical development programs, from initiation through completion of clinical trials, with inspection readiness in mind… more
