- University of Miami (Plantation, FL)
- …treating physician and University Clinical Research Staff. 5. Assists the Investigator obtain subject informed consent following the University Clinical Research ... and policies regarding reporting. 8. With input as required from the Investigator , assesses and documents adverse events and concomitant medications. 9. Works… more
- ICON Clinical Research (Cary, NC)
- …SQ) or any procedure necessary for the protocol as ordered by the investigator . + Attending investigator meetings, site initiation visits, and coordinator ... meetings to obtain training on drug preparation and administration and general knowledge about a protocol with a focus on clinical procedures. + Obtaining knowledge… more
- University of Michigan (Ann Arbor, MI)
- …expanding their clinical research portfolio, either in the form of investigator initiated clinical/translational trials and/or other clinical research activities for ... time and other support in order to initiate your own innovative, investigator -initiated studies. The Pediatric Oncology, BMT and Neuro-Oncology Program at Michigan… more
- Genentech (Boston, MA)
- …Lead Clinical Scientists will have interactions with external stakeholders, eg investigators , Therapy Area Experts (TAEs) and vendors. Alongside CSL, they may ... develop outlines for internal/external clinical presentations and communications (eg investigator meetings, study site interactions, patient information, newsletters); you… more
- Astellas Pharma (Northbrook, IL)
- …information and knowledge management, partnership and collaboration required in drug development. **Essential Job Responsibilities:** + Collaborates effectively with ... closely with safety officer in writing and/or reviewing Safety Narratives, Investigator Letters, and other safety documentation for site-reported safety events. +… more
- Pfizer (South San Francisco, CA)
- …resource for clinical issues raised by internal and external collaborators, investigators , consultants and contractors + Support and assist in the development ... development plans, INDs, annual reports, clinical study reports (CSRs), investigator brochures, statistical analysis plans, and regulatory documents. + Foster… more
- University of Michigan (Ann Arbor, MI)
- …growing research team. The Clinical Research Assistant will work with principal investigators and other research team members to accurately and efficiently carry out ... materials, and other relevant study documents for clinical studies. + Attend investigator meetings as a study team member and participate in recruitment strategies… more
- Lilly (Indianapolis, IN)
- …and review of clinical / regulatory documents (eg, protocols, Investigator Brochures, clinical study reports, briefing packages, etc.); collaborates ... clinical data in internal and external meetings, as needed (eg, DSMB, training, Investigator meetings, Board presentations, etc.) + Other duties as assigned or as… more
- Beth Israel Lahey Health (Exeter, NH)
- …Certification **Responsibilities:** 1. Collaborates with attending physicians and principal investigators to identify appropriate clinical trials for conduct and ... to administer investigational agents per protocol specifications. 2. Assists Principal Investigators (PI) in the process of assuring adequate informed consent.… more
- University of Utah (Salt Lake City, UT)
- …publication and grant-writing opportunities and will share in authorship and investigator status in a manner commensurate with their effort and responsibilities. ... record of helping scholars obtain independent funding as principal investigators of NIH funded K, F, and R01 awards....the successful completion of a criminal background check and/or drug screen. The University of Utah values candidates who… more