Clinical Trials Management Jobs in Rahway, NJ

About Our CompanyWere a physician-led patient-centric network committed to simplifying health care and bringing a more connected kind of care.Our primary multispecialty and urgent care providers serve millions of patients in traditional practices patients homes and virtually through VillageMD and ou...

Job DescriptionThe Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goa...

Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences) a distinguished department within our companys renowned Research and Development division quantitative scientists in partnership with other subject matter experts apply state-of-the art scientific methodologies and tools to enabl...

Job DescriptionAssociate Director Regulatory Submissions Archive OperationsLocation: Rahway NJ (Hybrid role - onsite 3 days per week required)Functional Area: Regulatory Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS)The Associate Director of R...

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 DescriptionOur company is dedicated to delivering innovations that extend and improve the lives of people worldwide. We are committed to supporting accessibility to medicine providing new therapeutic options and collaborating with governments and payers to help people who need our medicines and...

Job DescriptionOur company is dedicated to delivering innovations that extend and improve the lives of people worldwide. We are committed to supporting accessibility to medicine providing new therapeutic options and collaborating with governments and payers to help people who need our medicines and...

Job DescriptionThis is a hands-on pipeline project facing opportunity to be the primary day-to-day RCMCS lead to develop study design (DOE) statistical analysis and reported output using in-house developed JMP tools in fast-paced critical path projects. You will participate on process characterizati...

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 DescriptionUnder the minimal guidance of the Senior Director Business Development Execution the incumbent manages and is responsible for the business process and related activities associated with Global Regulatory Affairs and Clinical Safety (GRACS) Business Development Execution. The primary f...

Job DescriptionPosition Description:The selected candidate will provide procurement support for Clinical Development Sourcing and Procurement (CDSP) in Clinical Trial Central Labs. This includes sourcing of clinical services utilizing the Sourcing Management Process for strategic analysis of supplie...

Job DescriptionThe Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goa...

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...