- Mount Sinai Health System (New York, NY)
- …The **Project Manager II** will oversee the entire portfolio of Investigator-Initiated Clinical Trials (IICTs)/ Clinical Research Sponsor Collaboration (CRSC) ... implementing, and overseeing comprehensive training programs for new staff within the clinical research teams. This role ensures that new employees are… more
- WMCHealth (Valhalla, NY)
- Clinical Research Coordinator Company: NorthEast Provider Solutions Inc. City/State: Valhalla, NY Category: Clerical/Administrative Support Department: ... and pharmacist) and as the operational liaison for other research organizations, funding agencies and regulatory bodies....the protection of human subjects and the conduct of clinical research required. Knowledge of the International… more
- Mount Sinai Health System (New York, NY)
- … Trials Manager for Psychiatry works closely with the Vice Chair for Clinical Research to support the coordination and execution of investigator-initiated and ... Manager will work to ensure the operational success and regulatory compliance of a growing portfolio of research...RN, or related) preferred. * Minimum 5 years of clinical research experience, with at least 2… more
- FlexStaff (Lake Success, NY)
- …clinical trials. The CRC, RN ensures the accurate and timely conduct of clinical research , adhering to protocols, regulatory requirements, and patient ... **Req Number** 167969 FlexStaff is seeking a full-time Clinical Research Coordinator RN for our...concerns, as well as status of the protocol. + Monitor the overall day-to-day conduct of assigned studies in… more
- Bassett Healthcare (Cooperstown, NY)
- …creation, data maintenance and data analysis as needed + Maintain the Oncology Clinical Trials Research program's regulatory documentation + Maintain records ... Best-In-State Employer 2022! What you'll do The successful Oncology Clinical Trials Research Assistant will be highly...and efficient manner as required by internal and external regulatory and funding agencies + Assure appropriate data file… more
- IQVIA (West Seneca, NY)
- Internal Job Description **Job Title:** Clinical Research Coordinator **Work Set-Up:** Working On-site **Schedule** : 24 hours per week. **Responsibilities:** + ... sample collection including spirometry, and vital signs.** + Coordinate clinical research studies conducted by a supervising...licenses as required by company, country, state, and/or other regulatory bodies. + Working knowledge of clinical … more
- Touro University (Hawthorne, NY)
- … team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research . + Monitor study patients for adverse events in collaboration ... pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment,...to ensure protocol compliance in conjunction with the PI, clinical team and clinical research … more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval...Interacts with investigators and their staff to facilitate and monitor the conduct of multidepartment clinical studies.… more
- University of Rochester (Rochester, NY)
- …are resolved. Demonstrates accountability for initial and ongoing learning related to clinical research studies. + Keeps current with study-specific training, ... institutional policies. + Attends training sessions and other educational opportunities related to clinical research in order to learn and keep current with Good… more
- Catholic Health Services (West Islip, NY)
- …required information is complete, accurate, and readily available for clinical research audits or study sponsor monitor visits,i.e.: medical records, case ... education and information to study participants and families about clinical research participation and compliance. Discusses study...and other source documents. + Must be available during monitor site visits or audits to answer questions and… more