- Bristol Myers Squibb (Madison, NJ)
- …Competencies:** + Demonstrated applied knowledge of ICH/GCP, regulatory guidelines/directives, clinical research processes and principles of Quality Assurance ... effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback… more
- Sanofi Group (Morristown, NJ)
- …for interaction with regulatory authorities, approval of protocols, informed consent documents, clinical study reports, and product labels. In addition, the GPH ... goals, and objectives + Responsible for generating support and implementation of clinical studies + Ensures operational plans are integrated across all… more
- System One (Lindenwold, NJ)
- … Principal Investigator (PI) provides oversight and medical leadership for respiratory or pulmonary clinical research studies . This PRN role ensures all ... Job Title: Clinical Research Physician (Respiratory, PRN) Location... clinical staff; ensure GCP compliance. + Oversee study drug accountability and documentation. + Liaise… more
- J&J Family of Companies (Titusville, NJ)
- …+ End-to-end expertise in RWE studies including conceptualizing the research questions, data feasibility, study design, analysis, programming, and ... time-to-event analyses, external control arm studies , hybrid control arm studies , retrospective and prospective study designs. + Provide thought leadership… more
- Bristol Myers Squibb (Madison, NJ)
- …oversees evidence generation for the I&N portfolio, including Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and ... throughout study and support readout) + Should have experience in clinical concept development and partnering across the drug development continuum. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …of evidence generation book of work (including Medical Affairs Sponsored studies , clinical research collaborations, investigator-sponsored studies ... with stakeholders from Global Medical and International Medical Teams, Research & Discovery, Global Drug Development (GDD),...Cell Therapy MEG book of work (Medical Affairs sponsored studies , clinical research collaborations and… more
- PsychoGenics (Paramus, NJ)
- …needed superior clinical candidates to patients. PsychoGenics is seeking a Research Scientist (or Sr. Scientist, depending on experience) who will work closely ... severely disabling CNS and orphan disorders and reduce the attrition rate in clinical development. We are known for our cutting-edge translational approach to … more
- Sanofi Group (Morristown, NJ)
- …include interactions with regulatory authorities, approval of protocols, informed consent documents, clinical study reports, and product labels. In addition, the ... goals, and objectives + Responsible for generating support and implementation of clinical studies + Ensures operational plans are integrated across all… more
- Parexel (Trenton, NJ)
- …practice + Interact with clients and regulatory authorities + Review publications and clinical study reports + Travel to, attend, and actively contribute to ... describe advanced statistical techniques and interpret results + Familiarity with regulatory/ research guidelines on drug development, GCP, and statistical… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …medical evidence, (eg, observational studies , registries, and investigator-initiated studies (IISs) /investigator-initiated trials (IITs)) + Manage study ... design, execution, and reporting of studies to support generation of...relationships (eg, data & analytics partners CROs) + Track study progress, budgets, milestones, and ensure adherence to SOPs… more