- Merck (Rahway, NJ)
- …channels & decision-making processes between GCS and GCTO, including engagement with Clinical and Regulatory Organizations - communication channels + Monitor all ... of urgency and proactive approach to problem resolution + Understanding of regulatory frameworks in Clinical trials or clinical _supplies_ , GCP, GDP & GMP,… more
- BAYADA Home Health Care (Cherry Hill, NJ)
- …home care services. This role ensures that all care provided meets clinical standards, regulatory requirements, and organizational goals. The Clinical ... home visits to ensure adherence to care plans, nursing standards, and regulatory guidelines + Monitor clinical documentation for accuracy, timeliness, and… more
- IQVIA (Parsippany, NJ)
- …in lieu of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report… more
- Kelly Services (Bridgewater, NJ)
- ** Regulatory Specialist - Ad Promo (medical device)** Kelly(R) Science & Clinical is seeking a Regulatory Specialist for our client, a leading medical device ... laws and regulations for US and Canada. + Provides regulatory review and approval of advertising and promotional materials,...the Kelly Talent Community. Why Kelly (R) Science & Clinical ? Kelly Science & Clinical is your… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... - escalating quality issues as appropriate + Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query… more
- J&J Family of Companies (Titusville, NJ)
- …protocol, clinical trial materials, and takes ownership for the content of clinical study reports and relevant documents for regulatory filings. Team matrix ... project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management,… more
- J&J Family of Companies (Titusville, NJ)
- …protocol, clinical trial materials, and takes ownership for the content of clinical study reports and relevant documents for regulatory filings. Team matrix ... project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management,… more
- Bristol Myers Squibb (Madison, NJ)
- …of clinical trials and will supervise and have accountability for the clinical components of regulatory filings + Will contribute to overall strategy for ... a clinical development leader; with greater than 10 years of extensive clinical trial, drug development, and regulatory experience, in addition to a strong… more
- Bristol Myers Squibb (Princeton, NJ)
- …working with disease and lab scientists, as well as BMS members from clinical , medical, commercial, regulatory , and diagnostics. Individual will also engage with ... development process; including experience with implementing a biomarker strategy + Clinical protocol authoring and review of regulatory documents. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …board meetings as Early Clinical Development Physician; serves as Primary Clinical Representative in Regulatory interactions for early development projects + ... Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and… more