Clinical Research Associate Manager Jobs in Rahway, NJ

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...

Required Skills Minimum of 5 years of medical writing experience with a strong focus on publications Experience working in a pharmaceutical biotech or medical communications agency setting CMPP certification Job Description: Client has an exciting opportunity for a Principal Medical Wr...

Job DescriptionAssociate Principal Scientist Regulatory Affairs- OncologyAt our company we aspire to be the premier research-intensive biopharmaceutical company. Were at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people a...

Principal Medical Writer PublicationsClient 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 stori...

Principal Medical Writer PublicationsClient 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 stori...

Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance we ensure the safety and efficacy of our existing and pipeline products to produce safe effective innovative medicine.T...

Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance we ensure the safety and efficacy of our existing and pipeline products to produce safe effective innovative medicine.T...

Job DescriptionOur Clinical Research team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance we ensure the safety and efficacy of our existing and pipeline products to produce safe effective innovative medicine.Summary Focus and Purpose...

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

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

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

Job DescriptionJOB DESCRIPTION SUMMARYPrimary activities include but are not limited to:The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design coordinate monitor and report clinical laboratory and field studies that will support the regulatory approval of new compa...

Job DescriptionJOB DESCRIPTION SUMMARYPrimary activities include but are not limited to:The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design coordinate monitor and report clinical laboratory and field studies that will support the regulatory approval of new compa...

Job DescriptionJOB DESCRIPTION SUMMARYPrimary activities include but are not limited to:The Associate Principal Scientist is a DVM and/or PhD whose primary function is to design coordinate monitor and report clinical laboratory and field studies that will support the regulatory approval of new compa...

Job DescriptionRole Summary:The Global Senior Director Medical Affairs (GDMA) is a subject matter expert in their area of responsibility (eg defined tumor asset vaccine) and responsible for driving execution of the Global Medical and Scientific Affairs (GMSA) portion for their assigned Therapeutic A...