- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction with key ... and abroad, governmental, academic, community and industry organizations.The Senior Clinical Study Manager role is primarily a...and delivery of study team plan and milestones (eg protocol , eCRF/EDC, IXRS, Clinical Study Oversight Plan… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol , Good Clinical Practices (GCPs), ... appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH)… more
- University of Southern California (Los Angeles, CA)
- …/Off Study of patients. 9. Assists in training of other Coordinators. B. Protocol Administration 1. Determines patient eligibility a. Schedules necessary tests. ... experienced Registered Nurse and has a strong interest in clinical research. The role of the protocol ...for reporting to the IRB and promptly notifies Data Manager of occurrence of SAE. 5. Interacts with the… more
- University of Pennsylvania (Philadelphia, PA)
- …Job Title Clinical Research Coordinator A/B (Department of Surgery Research Administration ) Job Profile Title Clinical Research Coordinator A Job Description ... Summary The CRC A will assist in the management of multiple clinical trials and responsibilities in specific research area. Coordinate the screening of patients,… more
- University of Miami (Miami, FL)
- …from protocol development and initiation to study close-out. The Manager , Clinical Research Nursing provides leadership and training/mentorship in planning, ... Department of Clinical Translational Research Site is currently seeking a full time Manager , Clinical Research Nursing to work in Miami. The Manager , … more
- Veterans Affairs, Veterans Health Administration (Bronx, NY)
- …review of the EDRP application. Responsibilities This position serves as a Clinical Laboratory Scientist (CLS) in the Microbiology section of the Clinical ... proper identification; able to evaluate results of same according to establish protocol . Prepares smears and stains them with appropriate staining method. Must be… more
- Dana-Farber Cancer Institute (Boston, MA)
- … Research Manager is responsible for tracking and complying with clinical trial performance benchmarks; eg protocol and regulatory compliance, patient ... The ** Clinical Research Manager (CRM)** works within...resolution. + Assist the principal investigator in developing the protocol budget, in collaboration with Research Administration … more
- Mount Sinai Health System (New York, NY)
- …assist in the administration and plan of the research program. The Clinical Program Manager will report into the Associate Director, Myeloma Translational ... **Job Description** The Clinical Program Manager provides clinical...Office (TCI CCTO). In collaboration with the Executive Director, clinical trials investigators, and TCI CCTO Administration ;… more
- Dana-Farber Cancer Institute (Boston, MA)
- The Clinical Research Manager (CRM) will work within the GI Oncology clinical research program and manage the research team in the overall conduct of ... The CRM is responsible for tracking and complying with clinical trial performance benchmarks; eg protocol and...CRM will assist the principal investigator in developing the protocol budget, in collaboration with Research Administration … more
- Veterans Affairs, Veterans Health Administration (Albany, NY)
- …Service of the Albany VA Medical Center in Albany, NY. This Supervisory Clinical Laboratory Technologist provides supervision of the Microbiology Department in a 1C ... are consistent with accrediting agency standards and requirements. - Recommends policy/ protocol changes to correct deficiencies and improve the program. - Maintains… more
- Dana-Farber Cancer Institute (Brookline, MA)
- The Clinical Trials and Transplant Billing Manager plays a critical role in ensuring accurate and compliant billing for clinical trials and transplant ... with Clinical Trial Principal Investigators (PIs), Business Managers, and Clinical Research Coordinators to interpret protocol activity schedules for… more
- UTMB Health (Galveston, TX)
- Research Nurse Manager (Research Administration - Galveston) **Galveston, Texas, United States** **Hot** Nursing & Care Management UTMB Health Requisition # ... certification preferred (as applicable to assigned program(s)/project(s). **Preferred:** Certified Clinical Research Professional (CCRP) or Certified Clinical … more
- Lucile Packard Children's Hospital Stanford (Palo Alto, CA)
- Clinical Services 1.0 FTE, 8 Hour Day Shift At Stanford Children's Health, we know world-renowned care begins with world-class caring. That's why we combine advanced ... and purpose of the job. Reporting to the Director, the Ambulatory Site Manager integrates physicians, staff and operations of multiple specialties to practice within… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Directive, and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction with key ... abroad, governmental, academic, community and industry organizations. The Senior Clinical Study Manager role is primarily a...and delivery of study team plan and milestones (eg protocol , eCRF/EDC, IXRS, Clinical Study Oversight Plan… more
- University of Rochester (Rochester, NY)
- …monitors research activity to ensure compliance with Standard Operating Procedures and Good Clinical Practices. The Clinical Research Manager (CRM) is ... day to day oversight and management of the assigned Clinical Trials Office and the assigned staff. Manages the...challenges to assure study objectives are achieved according to protocol and projected time-lines. - Assumes leadership in … more
- Harvard University (Cambridge, MA)
- …related discipline. + Three or more years of related experience which must include clinical research administration or clinical research, or a combination of ... Skills: + Experience working with Institutional Review Boards for human clinical studies including protocol generation, continuing review, enrollment tracking,… more
- CSL Behring (King Of Prussia, PA)
- **The Opportunity** The Clinical Trial Supply (CTS) Senior Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the ... multi-year study lifecycle. The CTS Senior Study Manager independently leads clinical studies to ensure...clinical studies. + Gather and documents requirements for clinical supplies based on protocol attributes and… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …winshipcancer.emory.edu. **Winship is seeking qualified candidates for the Assistant Manager , Clinical Trials position.** KEY RESPONSIBILITIES: + Responsible ... process, and opening of appropriate studies. + Supports the protocol feasibility review process. + Tracks team metrics including...administration program required and six (6) years of clinical research experience, with at least four (4) years… more
- Northwell Health (Westbury, NY)
- **Req Number** 142953 Job Description Provides management of research administration at a clinical site(s) including monitoring the quality and accuracy of ... for clinical research sites for questions related to the protocol conduct protocol , regulatory document completion, study supplies, client scheduling,… more
- Stanford University (Stanford, CA)
- …and Quality & Compliance Manager will be responsible for leading the administration and regulatory compliance of clinical research within the Department of ... Clinical Research Project and Quality & Compliance Manager , Emergency Medicine (Hybrid Opportunity) **School of Medicine, Stanford, California, United States** … more
