Overview
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, maintain 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.
Responsibilities
Assists 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
- Maintenance of databases
Qualifications
Education/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
Pay Range
USD $26.07 - USD $37.27 /Hr.
Working Conditions
Risk of exposure to blood and body fluids. Must be able to lift, push, pull 0-20 pounds. Voluntary use of N95 permitted. May not enter isolation areas or provide COVID-19 care. Annual E required.
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