- Genmab (Hamilton Square, NJ)
- …for automation, design and implement solutions, such as automations for Clinical trial agreements, contract management, site management relates tasks, ... and utilized at a pace never seen before. Join Genmab as an Associate Director , Intelligent Automation, R&D Digital Products as part of our IT & Digital Team… more
- Genmab (Trenton, NJ)
- … operations departments to coordinate the planning, execution, and management of clinical trial activities across medical affairs functions Contribute to ... to the Global Medical Affairs Strategy Lead (MASL) the Director will be responsible for the development and execution...the value of disease/products with focus on payer and clinical decision-maker outcomes Lead the strategy team congress activity… more
- Genmab (Trenton, NJ)
- …part of our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director , USMA Solid Tumor Portfolio. This role will report to the VP/Head of US ... tumor therapies and relevant studies Provides US market input to Global clinical development and Global Medical Affairs programs, staying abreast of the evolving… more
- Genmab (Trenton, NJ)
- …products. Lead the Global Regulatory Team (GRT) and Submission Team(s). Participate in Clinical Trial Teams, as required for the assigned project(s). For ... New Jersey, US and Tokyo, Japan. Our commitment to diversity , equity, and inclusion We are committed to fostering...equity, and inclusion We are committed to fostering workplace diversity at all levels of the company and we… more
- Genmab (Princeton, NJ)
- …partner synopsis, protocols, statistical analysis plans, results meetings presentations and clinical trial reports Coordinate data transfers from/to business ... trial responsible statistician with responsibilities as described below. The (Associate) Director chips into clinical development strategies and plans. This… more
- Genmab (Princeton, NJ)
- …of years of experience and/or skills) Minimum of 15+ years of experience in clinical trial management and 10+ years of people management experience, leading ... support the Data Management, Statistics, Drug Safety, Medical and Clinical Pharmacology functions across one or more trial...from time to time by his/her supervisor. As Senior Director , Head of Programming, it is expected that the… more
- Genmab (Princeton, NJ)
- …ICMJE), and other guidance related to scientific data communication. Understanding of clinical trial design and execution, statistical methods and clinical ... authentic is essential to fulfilling our purpose. The Role The Associate Director of Medical Communications will be responsible for driving the medical… more
- Genmab (Princeton, NJ)
- …of all aspects of clinical drug development, with particular emphasis on clinical trial design, trial execution, and strong knowledge about the ... process of a program and/or study. Must understand the Clinical Trial matrixed process from research through...New Jersey, US and Tokyo, Japan. Our commitment to diversity , equity, and inclusion We are committed to fostering… more
- Genmab (Princeton, NJ)
- … clinical trial implementation, and oversight of all aspects of clinical development working closely with the Medical Director and other cross-functions ... high-quality and timely deliverables. You will report to Sr Director , Clinical Research Scientist. Responsibilities Lead or...Research Scientist. Responsibilities Lead or co-lead one or more clinical trial (s) in a therapeutic area for… more
- Bristol Myers Squibb (Princeton, NJ)
- …to support regulatory filings (as relevant); and developing/maintaining relationships with key clinical trial sites and investigators in the therapeutic area. + ... inspection-readiness and successful implementation of CAPAs. + Leading a multi-national team of clinical trial professionals, who are experts in the execution of… more
- Bristol Myers Squibb (Princeton, NJ)
- …programs. + Leads the Clinical Science team in the planning and execution of clinical trial activities to support the Clinical Development Plan for the ... studies within assigned area + May serve as a Clinical Trial Lead or Co-Lead as needed...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
- Bristol Myers Squibb (Princeton, NJ)
- …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data towards development + Serving as principal functional ... or industry setting including education where applicable + Extensive experience in clinical trial design and execution, biomarker development, and development… more
- J&J Family of Companies (Horsham, PA)
- …(eg, statistics, clinical pharmacology, etc.) + Monitor, review and analyze clinical trial data + Assist with investigation and acquisition of additional ... Director , Clinical Research Scientist (Oncology) -...more at https://www.jnj.com/ . For more than 130 years, diversity , equity & inclusion (DEI) has been a part… more
- Bristol Myers Squibb (Princeton, NJ)
- …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal ... in their personal lives. Read more: careers.bms.com/working-with-us . The Director will be the clinical lead to...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
- Bristol Myers Squibb (Princeton, NJ)
- …on major markets and key assets; adjust communications plans in accordance with clinical trial results/milestones and changes in the market healthcare landscape ... Professional (CMPP), and ISMPP active member highly desired + Understanding of clinical trial design and execution, statistical methods and clinical… more
- Bristol Myers Squibb (Princeton, NJ)
- …Include : + Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data analytics, ... easy to understand policies specific to medical affairs and clinical trial /research activities that empower the business...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
- Bristol Myers Squibb (Princeton, NJ)
- …the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses & ... the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses &… more
- Bristol Myers Squibb (Princeton, NJ)
- …and Central Monitoring team, responsible for supporting delivery of reliable clinical trial information for internal decision making, regulatory approval ... holistic community of practice centered on quality by design, clinical trial risk management, efficient issue management,...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
- Bristol Myers Squibb (Princeton, NJ)
- …(GDM)** **Functional Area Description** Global Data Management (GDM) is responsible for clinical trial data acquisition, data management and review, and medical ... degree preferred. **Experience Requirements** + At least 7 years of global clinical trial expertise, including specific experience with eCOA capabilities and… more
- Bristol Myers Squibb (Princeton, NJ)
- …Global Data Management (GDM) **Functional Area Description** GDM is responsible for clinical trial data acquisition, data management and review, and medical ... + Expert understanding of the drug development process and clinical trial execution. + Expert knowledge of...talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared… more
