Cancer Clinical Research Project Manager – Data Quality and Study Start- Up

Include - : Serve as 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 Clinical Research, Research Coordinator, Clinical, Associate, Research Associate, Coordinator, Healthcare

Design study. Develop and implement protocol for quality control. Create analytic files with detailed documentation. Select appropriate statistical tools for addressing a given research question. Implement data analysis through statistical programmin Data Science, Director, Cancer, Assistant, Science, Technology, Education

Include: Serve as 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 Clinical Research, Research Coordinator, Clinical, Oncology, Associate, Research Associate, Healthcare

Include - : Serve as 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 Clinical Research, Research Coordinator, Clinical, Oncology, Associate, Research Associate, Healthcare

Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. Oversee data management for research projects. Develop and Clinical Research, Research Coordinator, Clinical, Research, Coordinator, Leadership, Healthcare

Serve as 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 developin Research Coordinator, Clinical Research, Associate, Clinical, Coordinator, Research, Healthcare

Serve as 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 developin Clinical Research, Research Coordinator, Associate, Research, Clinical, Coordinator, Healthcare

Serve as 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 developin Clinical Research, Research Coordinator, Clinical, Associate, Research, Coordinator, Healthcare

Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Identify and implement changes to recruitment strategies when necessary. Determine eligibility of and gather c Clinical Research, Research Coordinator, Clinical, Associate, Research, Coordinator, Healthcare

Include - : Serve as 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 Clinical Research, Research Coordinator, Associate, Clinical, Research, Coordinator, Healthcare

Serve as 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 developin Research Coordinator, Clinical Research, Associate, Research, Clinical, Coordinator, Healthcare

Include - : Serve as primary contact with research participants, sponsors, and regulatory agencies. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate col Clinical Research, Research Coordinator, Clinical, Oncology, Pediatric, Associate, Healthcare

Cancer Clinical Research Coordinator 2 - Neurosurgery (Hybrid) The Stanford Cancer Institute (SCI) is one of an elite number of National Cancer Institute-Designated Comprehensive Cancer Centers in the country, and is a prominent, dynamic, and complex Clinical Research, Research Coordinator, Clinical, Neuro, Coordinator, Research, Healthcare

Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. Oversee data management for research projects. Develop and Research Coordinator, Clinical Research, Imaging, Psychiatry, Precision, Neuro, Healthcare

Research Duties (50%): Collect patient information by reviewing electronic medical records and organize data for analysis in retrospective research studies. Interface with patients in order to administer research questionnaires. Perform telephone or Clinical Research, Research Coordinator, Clinical, Research, Coordinator, Assistant, Healthcare

Screening, consenting, and enrolling patients for clinical studies of biological specimens including peripheral blood cells, blood plasma, and tumor tissues. Coordinating sample acquisition for patients enrolled on clinical studies of biological spec Clinical Research, Research Coordinator, Clinical, Assistant, Coordinator, Research, Healthcare, Education

Serve as the primary contact with research participants, sponsor, and regulatory agencies. Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to Clinical Research, Research Coordinator, Clinical, Associate, Coordinator, Research, Healthcare

Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing Clinical, Research, Associate, Coordinator, Healthcare

Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing Clinical Research, Research Coordinator, Clinical, Associate, Research, Coordinator, Healthcare

Palo Alto Veterans Institute for Research (PAVIR) is seeking a full-time Clinical Research Associate to work with the Principal Investigator, Dr. Molly Timmerman, and the rest of the research staff. The Clinical Research Associate will be responsible for practicing a standardized cognitive behavioral intervention as part of a federally-funded study of...