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Clinical Research Coordinator, MA
American Oncology NetworkClinical Research Coordinator responsible for managing oncology clinical trials and ensuring compliance with regulations. Administer patient care and document clinical research activities effectively.
Posted 8/1/2026full-timeFort Myers • Florida • 🇺🇸 United StatesMid-LevelSenior💰 $21 - $37 per hourWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates proficiency in managing clinical trials, including data collection, documentation of adverse events, and adherence to FDA guidelines. Familiarity with clinical trial management systems and electronic medical records is essential for effective study execution.
Highest-signal resume keywords
Clinical Trial ManagementData Collection and ReportingAdverse Event DocumentationElectronic Medical Records (EMR)Clinical Trial Data Entry Systems (EDC)
ATS Keywords
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Hard Skills
Clinical Trial ManagementData CollectionAdverse Event DocumentationFDA Guidelines ComplianceResearch Experience
Tools & Technologies
MS Office (Word, Excel, PowerPoint, Outlook)Electronic Medical Records (EMR)Clinical Trial Data Entry Systems (EDC)Clinical Trial Management Systems (CTMS)
Industry Keywords
Clinical TrialsInvestigational ProductsResearch Study ManagementProtocol Elements
About the role
Key responsibilities & impact- Responsible for the performance of the research study under the supervision of the Principal Investigator
- Administer and clinically manage an average of 5 clinical trials open to accrual annually
- Identify and explain key protocol elements and perform study tasks under direct supervision
- Document different types of adverse events under direct supervision
- Ensure proper storage, dispensing, handling and destruction processes for investigational products
- Collect, record and report accurate data and demonstrate per FDA guidelines
Requirements
What you’ll need- High school education required
- Some college is preferred
- Previous research or related medical science experience
- Proficiency in MS Office Word, Excel, Power Point, and Outlook
- Prior experience with electronic medical records (EMR)
- Prior experience with clinical trial data entry systems (EDC)
- Prior Clinical Trial Management Systems (CTMS) preferred
Benefits
Comp & perks- comprehensive health insurance with a robust provider network
- 401k, which offers a 100% match and investment options
- generous Paid Time Off (PTO) program
- flexible work options
- professional development programs and tuition assistance