Clinical Jobs in Rahway, NJ

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 DescriptionWe are searching for a Section Lead to join Oncology Early Development (OED). This is an opportunity to oversee clinical strategy for one third of our companys early development internal pipeline combined with the opportunity to lead and mentor cross-functional teams. The successful c...

Job DescriptionThe Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance w...

Job DescriptionThe Associate Director in Global Clinical Supply (GCS) Compliance is a subject matter expert and project leader responsible for advancing and sustaining GxP Quality Systems across GCS to ensure clinical supply operations are executed in a compliant inspectionready and riskbased manner...

Job DescriptionThe Associate Director Global Data Management & Standards (GDMS) Academy reports to the Head of Global Data Management & Standards (GDMS) Business Operations and leads the strategy and execution for GDMS onboarding and the global skill and knowledge development collaboration with GDM...

Job DescriptionBrief Description of PositionThe Senior Director Portfolio & Resource Operations (PROS) reports to the Head of Global Data Management and Standards (GDMS) Business Operations and serves as the lead responsible for the development and maintenance of the GDMS portfolio and resource mana...

Job DescriptionBrief Description of PositionThe Senior Director Portfolio & Resource Operations (PROS) reports to the Head of Global Data Management and Standards (GDMS) Business Operations and serves as the lead responsible for the development and maintenance of the GDMS portfolio and resource mana...

Job DescriptionThe Principal Trial Manager is responsible for leading projects and initiatives to improve the quality and compliance of the data management functional areas in addition to the regular responsibilities as an individual Trial Manager (TM). They will interact with Trial Managers as SME...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our Companys Oncology medicines span all phases of clinical development (pre-clinical to post-licensure)....

Job DescriptionJob Description:The Formulation Laboratory and Experimentation (FLEx) Center is a multi-modality (small molecule biologics vaccine) Drug Product development and clinical manufacturing facility in Rahway New Jersey. This team ensures right-first-time manufacture and delivery of high qu...

Job DescriptionPosition Overview:Under the direction of the applicable management the Clinical Data Manager (CDM) is responsible for executing end to end data management activities pertaining to clinical trials including but not limited to; data management tool and system development validation and...

Job DescriptionOur Research Laboratories 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 company mis...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our companys Atherosclerosis &...

Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Companys Oncology medicines span all phases of clinical development (pre-clinical to post-licensure...

Job Title: TP & Clinical SAS Developer Job Location: Upper Gwynedd PA & Rahway NJ (Onsite from day one) Job Duration: 12 months Minimum years of experience required: 5 years Type of Hire: w2 contract JOB DETAILS: have 6-8 yrs of exp in clinical domain knowledge of SDTM advanced SAS mac...

Job DescriptionCOA Sr. Specialist is responsible for providing end-to-end COA systems project management support including but not limited to gathering study-specific user requirements executing UAT tasks managing project timelines managing and enforcing COA systems Standards. COA Sr. Specialist als...

Job DescriptionJob SummaryThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the ophthalmology therapeutic area. Our companys ophthalmology medicines span all phases of clinical develop...

Job DescriptionPrimary activities include but are not limited to:Assumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle Veeva platforms along with the external data captured in support of the clinical studies.Coordinates and partic...

Job DescriptionThe Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs for oncology indications. The Associate Vice President will manage and oversee the entire cycle of clinical development including s...

Job DescriptionDirector (Ophthalmology) CRSCThe Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensure...