- Bristol Myers Squibb (San Diego, CA)
- …regulatory authority interactions, design, and execution of Phase 0 to Phase 3 clinical trials, and medical monitoring. This role provides medical direction and ... of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial… more
- University of Michigan (Ann Arbor, MI)
- …Concepts and Research Design 2. Ethical Participant Safety Considerations 3 . Investigational Products Development and Regulation 4. Clinical Study Operations ... team to coordinate and execute aspects of sponsor and/or investigator initiated clinical studies. These activities include, but are...from SoCRA or ACRP prior to applying.) + Minimum 3 years of directly related experience in clinical research… more
- University of Colorado (Aurora, CO)
- …informed consent documents as needed throughout the study + Facilitate process for investigator receipt and evaluation of external IND safety reports + Other duties ... working with Principal Investigators (PIs) + 1 year Project Management experience + 3 years of regulatory experience + IRB experience (COMIRB or central IRB, such… more
- US Tech Solutions (North Chicago, IL)
- …**Clinical Study Agreements, Confidential Disclosure Agreements, Master Agreements, Investigator Initiated Agreements, Service Agreements** ect In partnership with ... Communication Skills; providing updates across functions; written and verbally 3 . **Contractual or Paralegal** experience highly preferred **Responsibilities:** *… more
- Mount Sinai Health System (New York, NY)
- …field or be enrolled in a program preferred **Experience Requirements** + 3 years minimum demonstrated clinical and nursing expertise working in a staff ... in a manner that is acceptable to others and to the organization. ** Compliance ** - Assures compliance with regulatory, insurance and ethical standards regarding… more
- Mount Sinai Health System (New York, NY)
- …Masters in nursing or health related field preferred. Experience Requirements 3 years minimum clinical nursing experience with some Charge Nurse/supervisory ... aspects of Purposeful Hourly Rounding (PHR) and role models expected behaviors. 3 . Ensures the integration of PHR into clinical activities to enhance Relationship… more
- Mount Sinai Health System (Brooklyn, NY)
- …aspects of Purposeful Hourly Rounding (PHR) and role models expected behaviors. 3 . Ensures the integration of PHR into clinical activities to enhance Relationship ... RCA process and develops and implements corrective action plans. 3 . Fosters a fair and open culture that encourages...with staff and leadership about unit progress, changes, and compliance with quality and safety metrics. 6. Responds to… more
- Parexel (Annapolis, MD)
- …solutions. As a member of this team, you will be essential to ensuring our Investigator sites are prepared to start trials, with a focus on reducing Site Activation ... + Collects and reviews initial regulatory packets and site contracts for investigator sites. + Coordinate efforts for all site activation related activities… more
- Mayo Clinic (Phoenix, AZ)
- …survey, chart review) clinical research protocols with direction from the principal investigator and/or supervisor in compliance with regulatory laws and ... to secure your future. **Responsibilities** Receives direction from principal investigator , supervisor, or other staff involved in research protocol(s). Interacts… more
- ThermoFisher Scientific (St. Louis, MO)
- …Work:** Thermo Fisher Scientific Inc. is seeking a motivated and ambitious Deviation Investigator to join our world-class Manufacturing team in St. Louis. As a ... Deviation Investigator , you will play a crucial role in ensuring...pharmaceutical industry with progressively increasing responsibility + Experience with compliance , problem-solving, simple and complex root cause analysis tools… more