Senior Clinical Research Associate Jobs in Rahway, NJ

Job DescriptionThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area. Our companys Oncology medicines span all phases of clinical development (p...

Job DescriptionRole Summary:The Global Associate Director Medical Affairs (GADMA) has scientific and working knowledge in their area of responsibility (eg defined tumor asset vaccine) and responsible for supporting execution of the Global Medical and Scientific Affairs (GMSA) portion for their assig...

Job DescriptionRole Summary:The Sr. Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for Dermatology in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commerci...

Job DescriptionThe Sr. Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for Rheumatology in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization te...

Job DescriptionThe Executive Director Value & Implementation Global Medical & Scientific Affairs (V&I GMSA) Genitourinary Oncology position resides in the V&I organization which includes GMSA as well as Outcomes Research.This position referred to as EDMA is accountable for the alignment and executio...

Job DescriptionThe Executive Director Value & Implementation Global Medical & Scientific Affairs (V&I GMSA) Global Therapeutic Area (TA) position resides in the V&I organization which includes GMSA as well as Outcomes Research.This position referred to as TA EDMA is accountable for the alignment and...

Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and app...

Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and app...

Job DescriptionThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the insert name of TA therapeutic area. Our companys insert name of TA medicines span all phases of clini...

Job DescriptionThe 2-year Physician Scientist Program provides pharmaceutical medicine training and opportunities to physicians completing residency or fellowship with the goal of recruiting new talent and contributing to the organizations inclusion objectives. The program provides in-depth exposure...

Job DescriptionThe Breast Cancer Global Senior Director Medical Affairs (GDMA) is the breast cancer subject matter expert and responsible for driving execution of the Global Medical and Scientific Affairs (GMSA) portion for breast cancer as part of the Global Value & Implementation (V&I) Plans. As a...

Job DescriptionOur company in the United States and Canada is a global health care leader with a diversified portfolio of prescription medicines vaccines and animal health products. Today we are building a new kind of healthcare company one that is ready to help create a healthier future for all of...

Job DescriptionThe Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for atherosclerosis in key countries and regions. They are impactful members of Product Development Team sub-teams and Global Human Health commercialization tea...

Job DescriptionThe Associate Director Regulatory Affairs supports products in the Oncology therapeutic area as part of a regulatory team. The individual will have excellent communication and collaboration skills and will work closely with a global regulatory lead(s) to help develop and implement a g...

Principal Medical Writer Publications Client has an exciting opportunity for a Principal Medical Writer at an award-winning best-in-class in-house agency at a major pharma company. Join our newly established MCS Medical Communications Team-a dynamic start-up focused on redefining how scientific s...

Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development the Clinical Director will manage the entire cycle of...

Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development the Clinical Director will manage the entire cycle of...

Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development the Clinical Director will manage the entire cycle of...