Clinical Research Associate
About The Position
This role involves executing daily trial operations by overseeing day-to-day project protocols, design strategies, and monitoring workflows for complex clinical trials. The associate will safeguard data integrity by collecting and maintaining meticulous research records, case notes, and informed consents to ensure accuracy and compliance. They will also manage risk and resolutions by identifying, reporting, and resolving clinical protocol deviations and adverse events swiftly. Additionally, the role contributes to advancing scientific communication through medical literature publications and preparing high-level lecture reports and presentations for global conferences.
Requirements
- High School diploma equivalency with 2 years of cumulative experience OR Associate's degree/Technical degree OR 4 years of applicable cumulative job specific experience required.
- Clinical research experience
Nice To Haves
- Cardiology research experience
Responsibilities
- Oversee day-to-day project protocols, design strategies, and monitoring workflows for complex clinical trials.
- Collect and maintain meticulous research records, case notes, and informed consents to ensure absolute accuracy and strict compliance.
- Identify, report, and resolve clinical protocol deviations and adverse events swiftly to protect trial integrity.
- Contribute to medical literature publications and prepare high-level lecture reports and presentations for global conferences.
Benefits
- Paid time off (PTO)
- Various health insurance options & wellness plans
- Retirement benefits including employer match plans
- Long-term & short-term disability
- Employee assistance programs (EAP)
- Parental leave & adoption assistance
- Tuition reimbursement
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
