- 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 (Carlsbad, CA)
- …required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions * Perform site monitoring visits (selection, ... as appropriate. * Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF)… more
- 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
- 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
- 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
- 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
- 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
- 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
- ICON Clinical Research (Hickory, NC)
- …deliver an unprecedented model of predictability and standardization. **Quicker start -up** Our operational structure integrates centralized services, including but ... limited to site feasibility, patient recruitment, budgeting and contracting, with dedicated on-site services and flexible resourcing to streamline our processes and… more
- 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
Recent Jobs
-
Front Office Coordinator - Rehab Services - FT - Days
- LifePoint Health (Clyde, NC)