E-verify
Healthcare
ClinicalResearchAssociate
“Clinical Research Associate at E-verify. Skills: Clinical Trials, Site Monitoring, Data Management, Regulatory Compliance. Support site monitoring activities. Assist with data quality and query support”
What You'll Achieve.
Ensure protocol adherence; Ensure participant safety; Ensure data integrity
Industry & Context.
Problem Solving; Uses structured approaches to escalate issues; Identifies root causes; Distinguishes urgent vs. non-urgent issues; Brings potential risks to senior staff
Must complete federal Employment Eligibility Verification I-9 form, Must present acceptable and original documents to prove identity and work authorization, Criminal history background check required, May be required to report violations of law under Title IX and Clery Act
What They're Looking For.
Must Have
Bachelor's Degree in life sciences, nursing, public health or a related field, Basic understanding of GCP/Human Subjects Protection, Demonstrated ability to follow SOPs, maintain accuracy, and learn quickly
Nice to Have
Bachelor's Degree in life sciences, nursing, public health or a related field with at least 1 year of experience in clinical research support (CTA, CRC assistant, research intern), Experience with EDC/CTMS systems, Familiarity with risk-based monitoring concepts, GCP training (ICH E6) and institutional human subjects training upon hire, IATA certification if handling/shipping specimens, ACRP (CCRA, ACRP-CP) or SOCRA CCRP® certification
What You'll Do.
Support site monitoring activities
Assist with data quality and query support
Support essential document management
Aid in participant safety verification
Contribute to study start-up activities
Maintain study trackers and systems
Support investigational product documentation
Support audit and inspection readiness
How You'll Work.
Team & Collaboration
Works effectively with site teams, CRAs, and study staff; Communicates respectfully with CRCs and PI staff; Works closely with Clinical Research Coordinators, regulatory staff, data management teams, investigational pharmacy, and study leadership; Coordinates with vendors (IVRS/IWRS, central labs, eCOA)
Communication Scope
Written Communication; Clear, concise documentation; Drafts clear visit notes; Writes concise query explanations; Communicates respectfully; Adapts communication style
Process & Methodology
Planning tasks, Anticipating workload steps, Maintaining trackers for action items, Prioritizing data checks
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