- Bristol Myers Squibb (Madison, NJ)
- …+ Serves as a primary source of medical accountability and oversight for multiple clinical trials + Manages Phase I/II studies, with demonstrated decision making ... Monitoring** + Serves as an independent Medical Monitor for clinical trials from Phase 1 through Proof-of-Concept... development strategy + Analyzing, interpreting, and acting on clinical trial data to support development +… more
- Vitalief (New Brunswick, NJ)
- …working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong ... (GCP) guidelines. + Assist investigators (physicians) to prepare and implement new clinical trials , screens and enrolls study participants, and provides… more
- Bristol Myers Squibb (Princeton, NJ)
- …includes oversight of clinical monitoring, interpretation and analysis of all clinical trials and protocols in late-stage development, life cycle management ... clinical monitoring, interpretation and analysis of all clinical trials and protocols in late-stage development...critical discussions with health authorities in the interpretation of clinical data, clinical trial design… more
- Bausch + Lomb (Trenton, NJ)
- …support and guidance for the ongoing surveillance of the safety of patients in clinical trials by reviewing reported AEs and SAEs and assure proper reporting ... for training purposes. **POSITION REQUIREMENTS** **:** + Strong knowledge of Good Clinical Practices (GCP), clinical trials management (including site… more
- Stryker (Trenton, NJ)
- …guidelines, GCP, and regulatory requirements. This includes establishing and maintaining clinical trial databases, ensuring all data-related operations comply ... + Develop complex status reports, specifications for analysis of clinical trial data for interim and final...capture, and XML + Previous experience with complex, global trials . This role will be posted for a minimum… more
- J&J Family of Companies (Titusville, NJ)
- …input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes ownership ... Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filings**… more
- Merck (Rahway, NJ)
- … Sciences, Clinical Studies, Clinical Testing, Clinical Trial Development, Clinical Trials , Data Analysis, Drug Development, Ethical Standards, ... development strategies for investigational or marketed Oncology drugs. + Planning clinical trials (design, operational plans, settings) based on these … more
- Merck (Rahway, NJ)
- …Management, Clinical Studies, Clinical Testing, Clinical Trial Development, Clinical Trials , Communication, Data Analysis, Drug Development, ... strategies for investigational or marketed cardiovascular and respiratory drugs + Planning clinical trials (design, operational plans, settings) based on these … more
- Vitalief (Livingston, NJ)
- …working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong ... Proficiency in Microsoft Office and familiarity with electronic health records or clinical trial management systems. + A compassionate, professional demeanor,… more
- Vitalief (New Brunswick, NJ)
- …working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong ... business and domain expertise to provide more efficient, higher-quality clinical trials and unmatched value to Sponsors,...operations, and continually improving the success of our client's clinical trial outcomes. + Lead sales pursuits… more