Clinical Research Associate III at University Health Partners of Hawaii

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Full Time

Start Date

Immediate

Expiry Date

07 May, 26

Salary

0.0

Posted On

06 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Patient Enrollment, Data Collection, Medical Terminology, Problem Identification, Patient Safety Monitoring, Consent Assistance, Study Calendar Development, Adverse Event Monitoring, Protocol Knowledge, Data Management, Troubleshooting, Laboratory Coordination, Report Preparation, Medical Record Evaluation

Industry

Medical Practices

Description

POSITION SUMMARY Regular, Full-Time, RCUH Non-Civil Service position with the University of Hawai‘i Cancer Center (UHCC), Clinical Trials Office (CTO), located in Honolulu, Hawai‘i. Continuation of employment is dependent upon program/operational needs, satisfactory work performance, availability of funds, and compliance with applicable Federal/State laws. Facilitates patient enrollment into trials. Drives to transport specimens and to access hospitals on Oahu. Assists physician in obtaining consent. Assists with data collection and management. Develops study calendars and monitors patient safety. Reviews clinical data and identifies problems. Provides input on study continuation. Monitors for serious adverse events. Serves as a resource and troubleshooter for any trial-related problem. Develops specialized knowledge of clinical trial protocols. Attends meetings out of state and participates in the data management committees and tumor board meetings at local hospitals. Location: Hilo Benioff Straub Hospital ESSENTIAL JOB DUTIES AND FUNCTIONS * 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 QUALIFICATION REQUIREMENTS Education/Training/Experience Minimum: * 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. (Associate Degree from an accredited community college in a health-related discipline and three (3) years of clinical research experience may substitute for a Bachelor’s Degree.). * One to three (1-3) years of experience working in clinical research. Skills/Knowledge Minimum: * 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 * Employee assistance program (EAP) * Pet insurance with competitive premium rate UHP is an EEO/AAP Employer.

Responsibilities

Facilitates patient enrollment into oncology clinical trials and assists with data collection and management. Monitors patient safety and develops specialized knowledge of clinical trial protocols.