- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for the clinical operational and overall delivery and tactical execution of the clinical studies . The senior director will ensure a strong focus on competencies ... areas of opportunities to gain efficiencies and reduce timelines and costs for associated studies . They will work closely with Directors, Study Teams, and/or CRO… more
- Merck & Co. (Boston, MA)
- … will manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for...marketed Atherosclerosis drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as… more
- Merck & Co. (Upper Gwynedd, PA)
- …science that radically changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical ... Research Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the planning and directing of clinical research activities… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of Medical Affairs QA is ... across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director … more
- Merck & Co. (North Wales, PA)
- …retrospective database studies , assessment of patient reported outcomes, epidemiological studies and economic modeling.The Director also works closely with ... Job DescriptionJob purpose:Under the guidance of an Executive Director , within the Value and Implementation, Outcomes Research... Study Program Committee to evaluate outcomes research study protocols for studies in local markets.Supports… more
- Merck & Co. (Salt Lake City, UT)
- Job DescriptionPosition ResponsibilitiesThe Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert ... for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field… more
- Eisai, Inc (Nutley, NJ)
- …Phase IV clinical development and RWE programs for assigned products. Serve as a study lead on RWE studies . Create IIS strategies and review proposals in ... profile, we want to hear from you. The Medical Director will provide medical leadership for medical affairs strategy,...oversight of Phase IV clinical trial programs and RWE studies within the Medical Affairs department for products in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …indications.- Support as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study document ... research areas centered around rare diseases and immune disorders. SummaryThe Associate Director Global Medical Affairs Oncology (GMA), under the direction of the… more
- Eisai, Inc (Nutley, NJ)
- …difference. If this is your profile, we want to hear from you. The Director , US HEOR and RWE (field) is responsible for developing HEOR engaging population-based ... research activities and development of external communication materials. The Director facilitates coverage, reimbursement and appropriate utilization based on… more
- Merck & Co. (Rahway, NJ)
- …therapeutic area and encourages appropriate application of new methods to HEOR studies .Maintains responsibility to ensure study conduct is aligned with company ... Job DescriptionRole Summary:The Executive Director , Value & Implementation (V&I) Outcomes Research position resides in the V&I organization, which includes Global… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …meetings. May serve as medical lead for select company-sponsored evidence generating studies /projects. Manages all medical aspects such as study document ... as other research areas centered around rare diseases and immune disorders. SummaryThe Director US Medical Affairs (USMA) Oncology, under the direction of the Senior… more
- Merck & Co. (South San Francisco, CA)
- …Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology pipelines. - As ... an Associate Director , you will represent QP2 on cr o ss-...with external vendors and partners, on activities related to study design, protocol development, study execution, reporting… more
- Insmed Incorporated (San Diego, CA)
- …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , EDC Programming will lead and oversee EDC programming, and ... support clinical trials, ensuring data quality, compliance, and efficiency throughout the study lifecycle. The AD, EDC Programming will perform optimized EDC builds… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryAssociate Director , Global Medical Affairs Oncology Publications works with GMA Oncology ... Liaise with internal external authors, academic research organizations, and study investigators- Manage vendor budget and activities- Oversee the quality… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Executive Director , Data Management (Head of Global Data Management) sets the vision, ... units, regions, and functional areas to ensure successful outcomes for projects/ studies . This individual has sufficient understanding of regulations and GCP… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical Quality Assurance position is ... Independently conduct audits Review and oversee results of CQA audits of study sites, clinical vendors, clinical documents, and internal process audits Facilitate… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Executive Director , Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and academic ... to improve outcomes for patients. The EDSA leads a large investigator-initiated studies program in partnership with late-stage development teams in Medical Affairs… more
- Merck & Co. (Rahway, NJ)
- …leader to drive pipeline impact and lead a talented group of pharmacometricians.This director will be part of a leadership team responsible for applying traditional ... continue to innovate our pharmacometrics capabilities on a continuous basis. The Director will be accountable for directing a team of pharmacometricians with diverse… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Medical Director , US Oncology Medical Affairs - Women's Cancer assists in the development of medical ... the Medical Affairs department for assigned product(s). The Associate Medical Director utilizes expert medical, clinical and scientific knowledge in assigned… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive tactics ... for assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible for working with key stakeholders to develop and… more
Related Job Searches:
Associate Director Clinical Study,
Associate Study Director,
Chemistry Study Director,
Clinical Study Director,
Director,
Research Scientist Study Director,
Research Study Director,
Study,
Toxicology Study Director,
Toxicology Study Director Manager