Innovative research paves the way for improved patient outcomes. You can be a part of the research that’s driving new treatments and procedures at Legacy. In your role, you will recruit and screen study participants, maintaining billing and documentation and assist with regulatory preparation. If you’re ready to grow your skills and share in the Legacy mission of making life better for others, we invite you to consider this opportunity.
The position requires spending approximately two hours, one-on-one, with each study patient; performing a series of high quality clinical and experimental diagnostic tests, and interacting with them to maintain their long-term engagement in the study. It also requires recruiting and scheduling study subjects; and detail-oriented data cleaning and data management.
ResponsibilitiesAssists in the support of all aspects of clinical research studies including: Institutional Review Board and regulatory preparation, subject recruitment, screening, visit scheduling and preparation, study-specific billing sheets, source document maintenance, case report forms (CRFs) completion as appropriate, and maintenance of databases.
QualificationsEducation/Experience: Bachelor’s degree in a related field or equivalent healthcare experience.
Skills:
Proficient in word processing and spreadsheet management.
Excellent telephone diplomacy, verbal and written skills.
Organizational skills to manage multiple priorities and timelines.
Ability to keep accurate and detailed records.
Ability to assist in providing patient education following standard protocol.
Ability to adapt to change.
Ability to travel within the research community using personal or public transportation.
Ability to travel to developmental and promotional activities.
LEGACY’S VALUES IN ACTION:
Follows guidelines set forth in Legacy’s Values in Action.
Equal Opportunity Employer/Vet/Disabled
Compensation details: 26.07-37.27 Hourly Wage
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