- Stanford University (Stanford, CA)
- …both routine and complex. **Duties include:** + Participate with principal investigator in the preparation of the administrative components of proposals within ... submission process, both paper and electronic; review documents for completeness and compliance . + Develop, prepare, and finalize project budgets, and provide budget… more
- Actalent (Merced, CA)
- …develop flow sheets, and complete study documents/case report forms. + Ensure compliance with research protocols and review/audit case report forms for accuracy with ... with finance and management staff. + Interact regularly with the principal investigator to ensure patient safety and adherence to proper study conduct. +… more
- Idaho Division of Human Resources (Boise, ID)
- …2025/11/18 Posting End Date: 2025/12/02 Work Type: Full Time Remote: Flexible Hybrid Location: Boise, ID, United States Minimum Salary: 39.67 Maximum Salary: 40.50 ... include serving as the Tuberculosis Control Program Manager and Principal Investigator for the Tuberculosis Elimination and Laboratory Cooperative Agreement. The… more
- University of Michigan (Ann Arbor, MI)
- …the current study team to coordinate and execute aspects of sponsor and/or investigator initiated clinical studies. These activities include, but are not limited to: ... reports directly to ALK Program Manager, Clinical Lead, and Principal Investigator Supervision Exercised: None **Required Qualifications + Bachelor's degree in… more
- Bristol Myers Squibb (San Diego, CA)
- …of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial ... and regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits...ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines + Establish and maintain… more
- Bristol Myers Squibb (San Diego, CA)
- …to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and ... regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits...ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines + Establish and maintain… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …and assigned schedules. + Sets up experiments as prescribed by a principal investigator . + May be required to participate in laboratory maintenance activities such ... hazardous agents. + Performs related responsibilities as required by principal investigator . MINIMUM QUALIFICATIONS: + Bachelor's degree in a scientific field OR… more
- University of Michigan (Ann Arbor, MI)
- …the manager of the BRCF Epigenomics core, this individual will work independently on investigator projects as part of the fee for service activity. This includes but ... of the Epigenomics Core, this individual will work on investigator projects as part of the fee for service...ChIP-Seq. **Modes of Work** Positions that are eligible for hybrid or mobile/remote work mode are at the discretion… more
- University of Miami (Miami, FL)
- …of Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Hybrid Clinical Research Coordinator 2 to work at the UHealth Medical Campus in ... practice standards and clinical credentials as delegated bythe Principal Investigator .6. Monitors, documents, reports, and follows-up on study unanticipated/adverse… more
- Stanford University (Stanford, CA)
- …clinical studies and work under close direction of the principal investigator and/or study coordinator/supervisor. **Duties include:** + Serve as primary contact ... other study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols and review and audit case report forms for… more