Clinical Trials Jobs in Rahway, NJ

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...

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 DescriptionIn partnership with the Clinical Quality Operations Lead (CQOL and Head of CQO the CQOM is accountable for the execution of operational quality activities within the assigned therapeutic area. This includes operational quality management and inspection management activities.The CQOM w...

Job DescriptionWe are seeking three experienced and highly motivated individuals to join our team for a Clinical Operations Educator position. As Clinical Operations Educator you will be fully dedicated to training and education activities supporting the monitoring roles in clinical operations e.g....

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 DescriptionThe Global Clinical Supply (GCS) organization within our Research & Development Division manages the end-to-end clinical supply chain for the Companys portfolio (300 Phase I-IV Clinical Trials 200 Investigator Initiated Studies and 200 External Collaborations). GCS is accountable for...

Job DescriptionThe Global Clinical Supply (GCS) organization within our Research & Development Division manages the end-to-end clinical supply chain for the companys portfolio (300 Phase I-IV Clinical Trials 200 Investigator Initiated Studies and 200 External Collaborations). GCS is accountable for...

Job DescriptionThe Global Clinical Supply (GCS) organization within our companys Research Laboratories (manages the end-to-end clinical supply chain for the companys portfolio (300 Phase I-IV Clinical Trials 200 Investigator Initiated Studies and 200 External Collaborations). GCS is accountable for...

Job DescriptionThe Global Clinical Supply (GCS) organization within our companys Research Laboratories manages the end-to-end clinical supply chain for the companys portfolio (300 Phase I-IV Clinical Trials 200 Investigator Initiated Studies and 200 External Collaborations). GCS is accountable for t...

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 DescriptionJob Description:The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Companys biologics pipeline. We work closely with colleagues in Discovery Pre-clinical and Early...

Job DescriptionJob Description:The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance manufacturing processes for our Companys biologics pipeline. We work closely with colleagues in Discovery Pre-clinical and Early...

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 DescriptionOverviewThe Publication Specialist will work closely primarily withMedical Writers but also Publications Managers and Medical Communications Agencies as appropriate to facilitate the publication process to meet frequent submission deadlines for scientific publications/presentations ge...

Job DescriptionOur company is seeking a motivated individual to work as a bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a bioanalytical scientist position with primary duties in preparing and analyzing samples from biological matrices usin...

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 DescriptionTranslational Medicine (TMed) leverages multidisciplinary expertise to guide decision-making throughout the drug development process driving the most promising therapeutic candidates forward. We partner with stakeholders to strategically shape our pipeline and advance breakthrough med...

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...

Job DescriptionOur Research & Development Division Quality Assurance (QA) is an independent organization that provides quality focus at each critical stage of the product development life cycle including post approval marketing to ensure high-quality safe and effective products contributing to the c...

Job DescriptionThe Executive Director and Global Lead Patient Advocacy & Strategic Alliances position resides in the Value & Implementation (V&I) organization which includes Global Medical and Scientific Affairs as well as Outcomes Research. This position executes the patient engagement strategy in...