- Regeneron Pharmaceuticals (Warren, NJ)
- The ** Associate Manager Clinical Study ** (CSAM)... sites may be required to assist with monitoring clinical studies . **A typical day in this ... trial delivery. This role applies to internally sourced studies and studies outsourced to Clinical...of CROs deliverables will vary accordingly. The Assoc Mgr Clinical Study works with the study… more
- IQVIA (Parsippany, NJ)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …define ancillary and/or comparator supply strategy. + Develops plans for supplying clinical study sites with ancillary and/or comparator supplies, either through ... stability). **Supply Planning** + Serves as lead drug supply manager of a program and/or individual studies ...master kit lists. + Designs, reviews, and approves IP-related study tools (for clinical study … more
- Bristol Myers Squibb (Madison, NJ)
- …& completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database lock. **Position Summary** The Senior ... Manager , Clinical Data Management is a leadership...BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, … more
- Fresenius Medical Center (Jersey City, NJ)
- …or other site personnel + Obtains and updates essential documents for specific studies , as necessary + Attends clinical research-related training as required + ... + **Must have vehicle, as this employee will travel to multiple clinical sites.** + **Bilingual English/Spanish or English/Arabic, highly preferred.** PURPOSE AND… more
- Bristol Myers Squibb (Madison, NJ)
- …effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback ... TA, where deemed necessary. + Provide quality and compliance consultation to clinical trials teams throughout study lifecycle. + Provide regulatory intelligence… more
- Bristol Myers Squibb (Madison, NJ)
- …to lead structured benefit-risk assessments for assigned assets from early clinical development through late-stage and post-marketing. This role requires close ... relevant departments across the organization, including medical safety assessment, clinical development, global regulatory, epidemiology and others. The SBRA Lead… more
- VCA Animal Hospitals (Rutherford, NJ)
- …Doctors and the care team + Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits Benefits | VCA (vcacareers.com) _(open ... Join us as an ** Associate Veterinarian** at **VCA Rutherford Animal Hospital** and...dedicated pharmacy team of 1 controlled drug and inventory manager , 1 licensed pharmacy tech and 1 unlicensed pharmacy… more
- Merck (Rahway, NJ)
- …employees. **Key Responsibilities:** + Plan, conduct, and interpret pharmaceutical process development studies with manager and team support, such as scale up, ... technology transfer, design space development, clinical and stability batch manufacture, and process validation. + Apply problem-solving skills and aspects of… more
- Atlantic Health System (Morristown, NJ)
- …a Master's Degree in public health, healthcare, accounting, allied health, clinical -related studies , compliance, audit, computer science, finance, education, ... The Compliance and Privacy Manager oversees, in pertinent part, the following compliance...Draft responses to HIPAA-related regulatory inquiries. + Review business associate agreements, data use agreements, and limited data set… more