- University of Miami (Miami, FL)
- …manages day-to-day clinical research operations and study coordination duties, from protocol development and initiation to study close-out. The Manager, Clinical ... accuracy, organization, and integrity of clinical research documentation and protocol workflows. Identifies clinical safety implications during study development.6.… more
- University of Miami (Miami, FL)
- …studies. This role assists in the day-to-day operations of clinical research protocol implementation, and carries out study coordination duties from protocol ... protocols. + Collects, processes, packs, and ships specimens according to protocol , applicable standards and regulations. + Maintains study binders and filings… more
- Mount Sinai Health System (New York, NY)
- …research data. Prepares grant applications and documents and assists in protocol submissions (for eg, Institutional Review Board, Grants and Contracts Office). ... collection and management of patient clinical information, timely collection of protocol related samples including shipment to outside entities as required, obtain… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of the clinical research project. The RC coordinates aspects of protocol submissions, prepares and submits regulatory documents, and maintains records on ... School-affiliated hospitals. **Regulatory Compliance** + Prepares and submits all protocol applications, amendments, continuing reviews, and informed consent documents… more
- Logan Health (Kalispell, MT)
- …Acts as the main point of contact and resource for staff per department protocol and as applicable to assigned area(s). + Provides senior level administrative and ... supports financial and operational performance, and regulatory tracking per department protocol and as applicable to assigned area(s). + Coordinates and communicates… more
- Alabama Oncology (Birmingham, AL)
- Description of Duties: * Screens all potential patients for protocol eligibility. Maintains and submits monthly screening logs. * Presents trial concepts and details ... Coordinates study patient's scheduling for tests and treatments required by the protocol . * Documents any changes in the patient's condition, adverse events,… more
- J&J Family of Companies (Danvers, MA)
- …the FRS supports site selection and startup, drives patient recruitment, ensures protocol and data compliance, provides on call bedside technical/device support for ... clinical procedures, supports challenging technical/ protocol troubleshooting scenarios, critical software or product testing, and site closeouts. As a subject matter… more
- University of Washington (Seattle, WA)
- …expectation of additional projects in the future. **DUTIES AND RESPONSIBILITIES** ** Protocol Management - 50%** + With minimal guidance, implement research project ... FDA). + Develop, document and maintain procedures for patient registration and protocol implementation to ensure that research execution meets Good Clinical Practice… more
- Alaka'ina Foundation Family of Companies (Silver Spring, MD)
- …protocols submitted to the WRAIR, HSPB to include participating in project/ protocol development/modification. + Evaluate research protocols and protocol ... deviations, etc.) for compliance with relevant regulatory requirements and draft a Protocol Evaluation Form (PEF)/pre-review for each action received. + Reviews and… more
- Johns Hopkins University (Baltimore, MD)
- …or more senior research staff to ensure operational feasibility of proposed protocol /study design. + Develop standard operating procedures and data collection forms ... from protocol (s). + Develop consent form(s) for clinical trials based on protocol (s). + Prepare materials for submission to IRB. + Contribute to work with… more