- IQVIA (Troy, NY)
- …practice to senior staff. **Support Study Conduct By:** + Reviewing the study protocol , case report form (CRF), other study documents, and electronic data capture ... and documents. + Planning logistical activity for procedures as per protocol . + Generating volunteer instructions. + Identifying and obtaining required supplies… more
- Stony Brook University (Stony Brook, NY)
- …Nurse** for the Cancer Center Clinical Trials Department is responsible for the Protocol Management reviews for active and potential protocols. This, in large part, ... includes the determination of patient eligibility for protocol participation by way of chart review, data collection and patient evaluation/assessment… more
- Johns Hopkins University (Baltimore, MD)
- …and staff education needs are met with regard to assigned protocols. + Reports protocol deviations and adverse events in a timely manner. + Responsible for patient ... new protocols with PI/ sponsors. + Proposes and negotiates alternatives to improve protocol implementation. + Reviews and assesses new protocol for clarity,… more
- North Carolina State University (Raleigh, NC)
- …lead coordinators in coordinating multiple complex trials through the protocol life cycles of activation, implementation and closure. Other Work/Responsibilities: ... * Collect study data through a variety of methods, per study protocol (eg, administer surveys, observe/conduct study activities and record outcomes, electronic… more
- HCA Healthcare (Nashville, TN)
- …screening, enrollment and follow up of eligible subjects according to protocol requirements** + **Responsible for working with the principal investigator to ... of study patients by verifying informed consent procedures and adhering to protocol requirements/compliance** + **Ensures the integrity of the data submitted on Case… more
- Johns Hopkins University (Baltimore, MD)
- …seeking a **_Research Program Coordinator_** who will administratively coordinate clinical protocol implementation, typically for a single study. Will ensure the ... Coordinate all activities of a clinical research study to ensure adherence to protocol and validity of findings. + Participate in clinical study start-up meeting. +… more
- System One (Boston, MA)
- …Possess good judgment skills with ability to interpret information and protocol requirements, and initiate appropriate actions Assist Sr. Project Manager with ... Coordination/Implementation/Maintenance and Trial Close-out Assist in development of trial protocol IRB application and submit to appropriate authority; Assist in… more
- University of Southern California (Los Angeles, CA)
- …to research studies to investigators, research personnel, and subjects, from initial protocol design to completion of study and close-out report. The research ... and schedules assessments/tests/activities to meet research objectives and study protocol compliance. Communicates with study team personnel to ensure study… more
- Caterpillar, Inc. (Mossville, IL)
- …section is looking for a person to serve as a Data Link Strategy and Protocol developer. The Data Link Strategy and Protocol developer will perform a variety ... review data link strategy and protocols. + Collaborate with protocol requesters to review proposed designs and ensure that...ensure that all requests are complete and compliant with protocol design standards. + Serve as a trusted advisor… more
- IQVIA (Norwich, CT)
- …clinical research studies ensuring that studies are carried out according to protocol , contracted scope of work, good clinical practice, sponsor standard operating ... subjects to the study including the purpose of the study, procedures and protocol requirements such as timeline for visits + Maintains source documentation based on… more