Clinical Research Coordinator II
In all 50 statesFull-TimeMiddle
Salary not disclosed
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Job Details
- Languages
- Spanish, English
- Experience
- 2–3 years
- Required Skills
- GCP
Requirements
- Bachelor’s degree in a scientific, health-related, or behavioral field preferred
- 2–3 years of experience as a Clinical Research Coordinator or equivalent role
- Experience working with human subjects research required
- Working knowledge of GCP, informed consent requirements, and clinical research regulations
- Ability to manage study responsibilities independently
- Strong organizational skills with the ability to prioritize across multiple studies
- Excellent written and verbal communication skills in Spanish and English
- Experience using EDC systems, CTMS, and electronic health records
- Comfort working in a fully remote research environment
Responsibilities
- Independently coordinate assigned study activities in compliance with protocols, SOPs, GCP, and regulatory requirements
- Screen and evaluate potential research participants for eligibility
- Manage scheduling and execution of virtual and home-based study visits, assessments, and follow-up activities
- Collect, review, and enter study data accurately and in a timely manner using EDC systems
- Maintain complete, accurate, and audit-ready study documentation
- Conduct or support informed consent discussions in both Spanish and English
- Serve as a primary point of contact for research participants and caregivers
- Prepare for and support sponsor, IRB, and regulatory monitoring visits
- Track and report study metrics such as enrollment and retention
- Collaborate with investigators and cross-functional teams
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