- Novo Nordisk Inc. (Plainsboro, NJ)
- …you ready to make a difference? The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their role, they will lead ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR… more
- Merck & Co. (Rahway, NJ)
- …- #eligibleforERP GCSCareer25 #PSCSRequired Skills: Adaptability, Change Management, Clinical Research, Cross-Functional Team Leadership, Data Analysis, ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...business risks, & influence portfolio decisions with facts and data Demonstrates ability to balance strategy with ability for… more
- Merck & Co. (Rahway, NJ)
- … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and ... Primary activities include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose...Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet… more
- Merck & Co. (Lower Gwynedd, PA)
- …engineers, IT, Clinical , and QA, to turn operational and scientific data into trusted insights.- The PDMB Regulated Bioanalytics Department is seeking a ... Data Management Associate to join our LIMS...Data Management Associate to join our LIMS & Data ...will be utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings.… more
- Merck & Co. (Rahway, NJ)
- … clinical trial process: You can speak the language of protocols, specimens, and clinical data , and have a proven ability to translate scientific needs into ... Job DescriptionWe are seeking an Associate Principal Scientist to contribute to a pivotal...ecosystem. By automating workflows, powerful analytics, and stewarding these data , you will empower our scientists and clinical… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Director, Clinical Research Scientist will support and work predominately with ... and cross functional teams. This individual will provide scientific support to clinical development and operations, regulatory and quality assurance teams, as well… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …, and manage trial progress. Medical Monitoring: Provide medical oversight during clinical trials to ensure participant safety and data integrity.Review and ... OverviewThe Respiratory Clinical Development Medical Lead will oversee the ...interpret safety signals, adverse events, and efficacy data in collaboration with pharmacovigilance teams. Target Product Profile… more
- Insmed Incorporated (NJ)
- …other, and for the future of science, we're in. Are you?About the Role:The Clinical Trial Manager will be responsible for the management and oversight of phase I-IV ... clinical trials, with a key focus on Phase 1-2a,...timelines and deliverables. Key trial management support to the Associate Directors (CST Leads), as assigned.What You'll Do: Leads… more
- Merck & Co. (Upper Gwynedd, PA)
- …the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the ... Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial Development, Communication, Data Analysis, Decision Making, Drug Development,… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Associate Scientist will work with a multidisciplinary team of research scientists to investigate ... therapeutics for treating neutrophil-mediated diseases across several pre- clinical projects. This will involve assisting with tasks such as cell culture, in vitro… more
- Aequor (New York, NY)
- Description: Research Associate (Contractor) HTA Value & Evidence, Oncology, Global Access and Value, , Inc. Role Summary This is a full-time 12-month ... Contractor/Research Associate (RA) position in the HTA, Value & Evidence...the development and execution of deliverables to support early clinical development programs. The position is located at Headquarters… more
- CHRISTUS Health (Longview, TX)
- …new or innovative solutions. Leverages technology to facilitate the sharing of clinical performance or outcomes data . Creates mechanism for ensuring quality ... environment, which continuously supports improvement of operational, financial, and clinical components. Assumes primary responsibility for effective supervision of… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products.Principal… more
- Merck & Co. (Rahway, NJ)
- …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... members to ensure the quality and safe delivery of clinical supplies, the scientific rigor of the processes, and...IH sampling activities for new or existing equipment. Support data rich experimentation at pilot scale via process analytical… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Operations Associate as part of the Technical Operations team based in Raritan, NJ. ... operations team responsible for production of autologous CAR-T products for clinical and commercial operation in a controlled current Good Manufacturing Practice… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …contracts including vendor outsourcing agreements, PV Agreements (PVAs) and Safety Data Exchange Agreements (SDEAs). Maintains oversight of DSI contracts that are ... with key stakeholders within CSPV and external functions including Clinical Development, Research Development, Regulatory Affairs. Facilitate operational meetings… more
- Merck & Co. (North Wales, PA)
- …with Target; participation in Market Intelligence activities in connection with Target; data gathering and analysis in connection with Target; others that contribute ... meetings with Global Procurement in connection with supplier and stakeholder resolution; data gathering and analysis leading to short/medium term insights not in… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The… more
- Merck & Co. (Rahway, NJ)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategy, focusing on every touchpoint that impacts our customers. We leverage data and insights to inform our decision-making processes, ensuring that our ... and insight generation required; ability to navigate FRM/CRM portals and analyze data In depth knowledge of patient support programs, and experience collaborating… more
