- 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
- Olympus Corporation of the Americas (Center Valley, PA)
- …including facilitating the resolution of data queries under the guidance of the Clinical Research Associate (CRA), Data Management and/or the Clinical ... about Life at Olympus: https://www.olympusamerica.com/careers . **Job Description** The Sr. Clinical Trial Coordinator (Sr. CTC) will be responsible for supporting… 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. (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
- 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 (San Diego, CA)
- …understanding of CDISC standards (CDASH, SDTM) and regulatory requirements for clinical data .Experience with programming languages such as SQL, SAS, ... future of science, we're in. Are you?About the Role:The Associate Director, EDC Programming will lead and oversee EDC...the development and implementation of EDC systems to support clinical trials, ensuring data quality, compliance, and… 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)
- …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
