- Eisai, Inc (Nutley, NJ)
- …your profile, we want to hear from you. Job Summary Job Summary The Clinical Trial Assistant will support all phases of clinical study activities (feasibility, ... and close-out) under the direction and supervision by study Clinical Operations Lead(s). Plans, support , creates, and communicates...in program. This position may be office-based (hybrid) or remote based. For remote based, the selected… more
- Genmab (Plainsboro, NJ)
- …leading a small team to complete various programming efforts within a clinical trial.You will be responsible for ensuring integrity, consistency, and adherence to ... standards, and ensuring well-structured, high quality data summaries for internal decision making and reporting to health authorities. You will report to the… more
- Merck & Co. (North Wales, PA)
- …to engage key stakeholders.Demonstrated success in the assurance of deliverable quality and process compliance.Familiarity with statistics and clinical data ... 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment.MS (preferred) in Computer Science, Statistics, Applied Mathematics,… more
- Merck & Co. (Rahway, NJ)
- … Trials Regulation of the European Union). Responding to internal and clinical review comments on public disclosures; amending disclosures as appropriate ... internal and external reviewers, and guiding the posting through review and approval. Collaborating with clinical teams,...finalizing for posting on public websites; and addressing NIH Quality Analysis review comments to resolve issues… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … and provide comments to trial outlines/protocols for Novo Nordisk-sponsored clinical trials Review proposals for investigator-sponsored studies (ISS) and ... find better and more innovative ways to improve their quality of life. We're changing lives for a living....Medical Affairs team on relevant disease state topics and clinical trial data. Review and approve resources… more
- Merck & Co. (North Wales, PA)
- …for related drug/vaccine projects in Late Development Statistics.Interacts with Clinical , Regulatory, Statistical Programming, Data Management, and other company ... Research Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine projects.… more
- Merck & Co. (North Wales, PA)
- …the safety and efficacy claims of potential medical breakthroughs. Review the quality and reliability of clinical studies using deep scientific knowledge, ... statistical analysis and high- quality data to support decision making in ...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Durham, NC)
- …of Quality Notifications (QNs) and Change Requests (CRs).- Author, review , and approve SOPs. Assume project management opportunities, by leading and ... Job DescriptionSenior Specialist, Quality Systems and Compliance (P3) Our company is...establishing processes that ensure required safety guidelines are followed.- Review and approve qualification/validation documents for equipment and process… more
- Merck & Co. (Rahway, NJ)
- …and posters/oral presentations that report results from our company's General Medicine clinical trial program, as well as select early-stage development projects and ... collaborate with our Research & Development Division colleagues from Global Clinical Development, the Center for Observational and Real-World Evidence, Global… more
- Merck & Co. (North Wales, PA)
- …efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, ... and high- quality data to support decision making in clinical trials.-The Associate Principal Scientist, Statistical Programmer supports the design, development,… more
