• (Senior) Clinical Research Associate…

    IQVIA (Carlsbad, CA)
    …required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions * Perform site monitoring visits (selection, ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (07/14/25)
    - Related Jobs
  • Clinical Research Associate - Sponsor

    IQVIA (Parsippany, NJ)
    …required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions * Perform site monitoring visits (selection, ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (07/08/25)
    - Related Jobs
  • Project Manager II - Investigator Initiated…

    Mount Sinai Health System (New York, NY)
    …the entire portfolio of Investigator-Initiated Clinical Trials (IICTs)/Clinical Research Sponsor Collaboration (CRSC) within the organization. This role involves ... coordinating all aspects of trial management, ensuring compliance with regulatory requirements, and facilitating collaboration among multidisciplinary teams to meet… more
    Mount Sinai Health System (07/09/25)
    - Related Jobs
  • Regulatory Coordinator - Gynecologic…

    Dana-Farber Cancer Institute (Brookline, MA)
    …each assigned study in compliance with study sponsor requirement; Industry sponsor , DF/HCC sponsored etc. + Maintains various regulatory tracking databases ... all required deviation, violation, exception or other event reporting. Ensure various regulatory reporting required are met; Study Sponsor , FDA, IRB etc.… more
    Dana-Farber Cancer Institute (07/23/25)
    - Related Jobs
  • Director, Research Finance and Compliance

    St. Luke's University Health Network (Allentown, PA)
    …Luke's are our most valuable asset! Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering ... provides strategic and operational leadership for the financial management, regulatory compliance, and long-term sustainability of SLUHN Clinical Trials and… more
    St. Luke's University Health Network (07/29/25)
    - Related Jobs
  • Clinical Research Monitor

    General Dynamics Information Technology (Fort Detrick, MD)
    …**The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to ... actions (CAPAs)** **Submit documents to be filed in the sponsor 's regulatory file.** **Follow-up on monitoring visit...obtain a favorable NACLC T3 security investigation prior to start date.** **WHAT GDIT CAN OFFER YOU:** **Challenging work… more
    General Dynamics Information Technology (07/24/25)
    - Related Jobs
  • Registered Nurse RN Clinical Research Specialist

    Banner Health (Mesa, AZ)
    …Full-time, exempt, 40hrs week. Monday - Friday between 7-6pm (flexible with start /end times) Located on an 80-acre campus in Mesa, Arizona, Banner Desert ... abundance of exceptional opportunities with more than 700 licensed beds, including over 100 dedicated to children and 76 dedicated to our NICU. Areas of… more
    Banner Health (07/24/25)
    - Related Jobs
  • Associate Director Continuing Education, TMI

    Colorado State University (Fort Collins, CO)
    …candidates must be legally authorized to work in the United States by the proposed start date; the department will not sponsor a visa for this position. A ... TMI ). These facilities include 11,000+ square feet of dedicated CE space in addition to shared use of...to work in the United States by the proposed start date; the department will not sponsor more
    Colorado State University (07/04/25)
    - Related Jobs
  • Senior Director (Medical/MD) - ExploR&D…

    Lilly (Boston, MA)
    …study conduct including study design, safety management plans, protocol writing, regulatory documents, CRO interactions, study start up, investigator ... regulatory personnel to ensure compliance + Serve as Sponsor physician for case-management of SAEs, or provide oversight...candidates) + 25% travel may be required Lilly is dedicated to helping individuals with disabilities to actively engage… more
    Lilly (06/14/25)
    - Related Jobs
  • Clinical Research Point Coordinator Open Rank…

    University of Colorado (Aurora, CO)
    …initial site selection through budget negotiation, operationalization, organizational and regulatory approvals, and site activation to prepare completely for ... to problem solve and push forward startup activities efficiently to meet sponsor timelines. + Delegates startup tasks to other assigned team members and/or… more
    University of Colorado (07/23/25)
    - Related Jobs