- University of Miami (Miami, FL)
- …compilation, and documentation of research data related to the assigned research studies . The incumbent also assists with the implementation of daily study ... Organizes and handles the flow of information to and from study participants, including study participant contact information. Maintains consent… more
- Vitalief (Newark, NJ)
- …provides operational and administrative support for interventional oncology clinical research studies conducted at a leading academic research center in Newark, NJ. ... and institutional requirements. + Provide operational support across the full study lifecycle, including start-up, active conduct, and close-out activities. + Assist… more
- Avispa Technology (Palo Alto, CA)
- …primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. * Determine eligibility of and ... gather consent from study participants according to protocol. Assist in developing recruitment...Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case… more
- Department of State - Agency Wide (Stamford, CT)
- …with production figures, status of projects, and cost of operations. Designs, studies , and develops qualitative and quantitative data in support of management ... hours is equivalent to 1 full-time year of graduate study (your school and department determine what constitutes 1...determine what constitutes 1 full time year of graduate study ). The percentage of specialized work experience and the… more
- ThermoFisher Scientific (Greenville, NC)
- …clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the ... moderate to high complexity, and may assume regional lead or Clinical Study Manager responsibilities. **Essential Functions:** + Manages all aspects of monitoring… more
- Cleveland Clinic (Cleveland, OH)
- …team has the knowledge, guidance, and resources necessary to conduct innovative studies aimed at refining treatments, medical services, and more, helping advance our ... quality and safe patient care, anticipating and resolving patient care and study issues by serving as a liaison between investigators, research personnel, outside… more
- Arkansas Children's (Little Rock, AR)
- …Information:** The Clinical Research Nurse Coordinator coordinates of clinical research studies . Serves as a resource for research study participants, ... members of the clinical research team regarding specified aspects of the study . The Clinical Research Nurse upholds standards for human subjects protection.… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …early- and late-phase clinical trials. This role involves collaboration with cross-functional study teams where you will lead the design of complex imaging ... pipeline. + Provide leadership during the strategy phase of study design, guiding the team on all imaging aspects...ensure the delivery of high-quality imaging data in clinical studies . This includes drafting imaging manuals and other documents… more
- Sumitomo Pharma (Montgomery, AL)
- …Duties and Responsibilities** + Responsible for and lead all activities related to clinical study design from clinical study concept to clinical study ... complex decisions + Leads and drives strategy for clinical studies for assigned asset(s) within the Ophthalmology therapeutic area...reporting + Provide clinical input for and participate in study set up and design including data collection tools,… more
- System One (Rochester, NY)
- …Responsibilities The clinical Research Coordinator will manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including ... participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study … more