Clinical Research Associate III facilitating oncology clinical trials at the University of Hawai‘i Cancer Center. Enrolling participants and ensuring compliance with study protocols.
Responsibilities
Facilitates oncology clinical trials by enrolling eligible participants in available clinical trials and fulfilling data requirements for each trial.
Reviews clinic schedules and medical records of potential clinical trial participants, matching patient characteristics with eligibility requirements of available protocols.
Assists physicians and cancer care staff in coordinating laboratory tests/procedures required for pre-study testing.
Drives to transport specimens and to access hospitals on Oahu.
Assists physician in obtaining consent before enrolling a patient on a study.
Assists with patient education regarding the specific protocol patient will be registered to.
Responsible for all protocol data collection, including completing initial study forms, treatment forms, and follow-up forms.
Enters all patient tracking information into OnCore Clinical Trials Management System and/or other required data capture systems in a timely manner.
Reviews data for accuracy and submits data within time requirements and electronically if required.
Develops study calendars and monitors patient safety.
Reviews clinical data and identifies problems.
Provides input on study continuation.
Monitors for serious adverse events per Federal and/or sponsor guidelines, within the time parameters.
Serves as a resource and troubleshooter for any trial-related problem.
Develops specialized knowledge of clinical trial protocols grouped from a specific National Cancer Institute (NCI) research base or other source, or by disease site, etc.
Develops specialized knowledge of specific cancer care sites conducting clinical trials and/or job areas, such as education/training, regulatory, investigational drug accountability/storage, specimen collection/processing, database maintenance/reporting, and auditing.
Attends meetings out of state and participates in the data management committees and tumor board meetings at local hospitals.
Performs other duties as assigned.
Complies with all legal requirements and company policies
Requirements
Bachelor’s Degree from an accredited four (4) year college or university in a science or health-related field, such as Nursing, Medical Records, Medical Technology or Pharmacology, or other related field.
One to three (1-3) years of experience working in clinical research.
Knowledge of the practical and potential value of health care research.
Firm knowledge of medical terminology and medical records structure.
Ability to prepare written reports of study results and analyses.
Ability to evaluate and analyze existing techniques and procedures.
Ability to interpret, integrate, and correlate medical information from multiple sources (e.g., primary medical records, reports, and treatment records).
Ability to translate technical medical information in writing into lay language.
Benefits
Retirement plan with 3% dollar-for-dollar company matching contributions
Research Analyst conducting comprehensive surveys of voluntary mental health and substance use services in BC. Supporting data - driven policy advocacy for CMHA BC.
Senior Director, Equities Research Analyst analyzing market - related equity data to advise on growth - oriented investment opportunities. Working with the firm's portfolio managers on equity portfolios.
Research Specialist performing defined research and laboratory tests at Emory University. Collaborating with principal investigator and maintaining laboratory equipment and supplies.
Lead Research Analyst involved in research for KYC compliance and financial risk mitigation. Collaborating with global teams and analyzing data from multiple sources in a multilingual environment.
Research Analyst at DPR Construction analyzing data and delivering insights for compensation and benefits strategies. Collaborating with stakeholders to ensure data - driven decisions.
Research Associate delivering cutting - edge energy analytics and strategic insights in Australia’s energy sector. Engaging with clients and contributing to the global research team’s efforts.
Vice President Equity Research Analyst leading fundamental analysis for assigned companies in the Australian Small Cap Industrials Equity Research team. Mentoring junior analysts and providing insights to institutional investors in Sydney or Melbourne.
Technology Research Analyst investigating disruptive technologies in aerospace while collaborating with cross - functional teams. Contributing to strategic R&D initiatives and influencing next - generation product development.
Postdoctoral Research Associate at CCRM conducting research in reproductive biology and bioinformatics. Collaborating on understanding ovarian aging and its impact on fertility and disease.
Senior Clinical Research Associate managing clinical trials for Thermo Fisher Scientific in Germany. Conducting site monitoring, ensuring compliance, and maintaining data accuracy across multiple locations.