- Prime Healthcare (Passaic, NJ)
- …section(s) quality management/assurance program, 6) ensures compliance with all regulatory and accreditation requirements, 7) assesses staff competency and completes ... Connect With Us! (https://careers-primehealthcare.icims.com/jobs/219971/ clinical -lab-scientist-iii blood-bank/job?mode=apply&apply=yes&in\_iframe=1&hashed=-336024306) FacilitySt.… more
- Prime Healthcare (Denville, NJ)
- …section(s) quality management/assurance program, 6) ensures compliance with all regulatory and accreditation requirements, 7) assesses staff competency and completes ... Connect With Us! (https://careers-primehealthcare.icims.com/jobs/218925/ clinical -laboratory-scientist-iii/job?mode=apply&apply=yes&in\_iframe=1&hashed=-336024306) FacilitySt. Clare's… more
- Virtua Health (Marlton, NJ)
- …with certification within 12 months of hire. Refer to the Educational/ Regulatory Requirement (Department Specific) policy in the Nursing Administrative Manual. ... Virtua Health, a Magnet-recognized health system ranked by US News and World Report, has received many awards for quality, safety, and its outstanding work environment. As a High Reliability Organization, Virtua Health has systems in place that makes us… more
- Virtua Health (Voorhees, NJ)
- …Department positions. Enhances skills through ongoing education and training. Maintains regulatory and departmental level competencies. Hourly Rate: $18.33 - $27.47 ... The actual salary/rate will vary based on applicant's experience as well as internal equity and alignment with market data. Virtua offers a comprehensive package of benefits for full-time and part-time colleagues, including, but not limited to:… more
- United Therapeutics (Trenton, NJ)
- …Knowledge of data entry processing, from start to finish (QC, medical review, regulatory submissions) + Prior clinical or post marketing experience **Job ... in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports), OR + Master's...in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports) + 3+ years… more
- AbbVie (Jersey City, NJ)
- …Programming must effectively interface with Statistics, Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations. Responsibilities: + Leads ... sets for individual studies and integrated data. + Creates documentation for regulatory filings including reviewers guides and data definition documents. + Leads the… more
- Sumitomo Pharma (Trenton, NJ)
- …colleagues across the SMPA organization including, but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data ... as required. + Coordinate responses to ad hoc safety issues such as regulatory authority, site, or health care professional requests, along with PV physician,… more
- Merck (Rahway, NJ)
- …Develop deep business acumen and expertise in data and data standards across Clinical Development, Medical Affairs, and Regulatory Affairs domains. . Apply ... Information Architecture (BIA) group within our Research & Development Division's Clinical Development and Digital Solutions (CDDS) value team, the Business Strategy… more
- RWJBarnabas Health (Belleville, NJ)
- …required by the Rutgers Cancer Institute, the Hospital(s), the School/ Department and regulatory bodies. + Participate in clinical research + Attend to other ... and imaging equipment, and engages in academic activity by supporting clinical research protocols and participating in teaching activities. Responsibilities of the… more
- Taiho Oncology (Princeton, NJ)
- …internal stakeholders on mapping out the primary publication plan for scientific and clinical studies in process, prior to regulatory submissions, and assessment ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more