- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and ... regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology.Oncology expertise requiredClinical safety … more
- Merck & Co. (Rahway, NJ)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
- Merck & Co. (Rahway, NJ)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,...compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical … more
- Merck & Co. (Rahway, NJ)
- Job Description Role Summary: The Global Senior Director Medical Affairs (GDMA) is a subject matter expert in their area of responsibility (eg, defined tumor, ... Serves as the medical representative within Product Development sub-teams (including Clinical , V&I, Commercial, Publications, and Label), leveraging the GMSA vision… more
- Merck & Co. (Rahway, NJ)
- … to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study ... with key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical ...clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
- Merck & Co. (Rahway, NJ)
- …involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of ... monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director May Be Responsible For:Evaluating pre- clinical and translational… more
- Merck & Co. (Rahway, NJ)
- …principles to enhance patient safety and product usability. The Senior Director will champion enterprise-wide HF strategy, foster cross-functional ... Job DescriptionThe Senior Director of Human Factors (HF)...to the HF team and key stakeholders across R&D, clinical , regulatory, marketing, manufacturing, and quality functions.Educate and build… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …In addition, this position interacts with internal and external stakeholders for clinical safety matters and provides mentorship in talent development for ... safety issues supporting Global Medical Safety Lead. Responsible for safety governance/oversight of Clinical Safety and risk management activities… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, US and Global Brand Team, and US ... compound under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical...Product Team to inform clinical development, commercialization, market access, and other cross-functional strategic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …function as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, and Global Product Team to inform ... model the way and enable the team to act.Provides medical leadership to:- GMA clinical operations teams as part of evidence generation forums and study teams for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director ... centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of Medical Affairs QA is… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …and demand integrity and respect in all we do, create and deliver. Director , Clinical Development, will be responsible for the leadership, oversight, and ... age, national origin, protected veteran status, disability or any other legally protected status. Director , Clinical Development Base Salary Range: $180K - $240K more
- Parexel (Trenton, NJ)
- …across a broad spectrum of diseases. Overall responsibilities of the Associate / Medical Director are to: - Provide medical and safety monitoring for assigned ... clinical protocols, Medical Monitoring Plans (MMP), integrated clinical and statistical summary reports, safety plans,...sponsorship as needed with the support of the designated Senior Medical Director / Global Head of TA… more
- Integra LifeSciences (Princeton, NJ)
- …training programs for US-based healthcare customers. Under the guidance of the Director of Professional Education this will include planning, execution and budget ... external stakeholders to include Marketing, Legal, Compliance, Field Sales Leadership, Clinical Specialists, Medical Affairs, and HCP Faculty. **ESSENTIAL DUTIES AND… more
- Merck & Co. (Rahway, NJ)
- Job Description Role Summary The Associate Director of Procurement for Capital Projects will be responsible for overseeing and managing procurement activities for a ... ensuring compliance with company policies and processes. - Reporting to the Director of Capital Procurement Project Execution within the Global Capital Procurement… more
- Merck (Rahway, NJ)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,...compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical … more
- Merck (Rahway, NJ)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May Be Responsible For:** + Evaluating pre- clinical and… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …lead the clinical development activities in support of domestic and international clinical development initiatives. The Senior Director , GCD works in a ... clinical trials and regulatory filing activities. The Senior Director , GCD is responsible for all...potential for meeting an unmet medical need, establishing early clinical safety and proof of concept, conduct… more
- Sumitomo Pharma (Trenton, NJ)
- …seeking a dynamic, highly motivated, and experienced individual for the position of Senior Medical Director , Clinical Research (Ophthalmology) to join our ... working with the safety group to ensure adequacy of safety monitoring and reporting + Provide clinical input for and participate in study set up and design… more
- J&J Family of Companies (Titusville, NJ)
- …profoundly impact health for humanity. Learn more at https://www.jnj.com/. **POSITION SUMMARY:** The Senior Director , Clinical Leader (CL) is responsible for ... supplies unit, data management, medical writing, biostatistics, global medical safety , pharmacogenomics, early clinical development, clinical pharmacology,… more
