Bilingual Clinical Research Coordinator II
Overview
Clinical Research Coordinator II leads study coordination and subject management across multiple trials. This role serves as primary liaison between investigators sponsors and clinical staff ensuring protocol compliance and regulatory standards. Responsibilities include managing concurrent trials scheduling volunteers and maintaining accurate study documentation.
What You'll Do13
- 1Develop strong working relationships and become point of contact for clinic and sponsor
- 2Manage multiple concurrent trials and assist with mentor training
- 3Maintain study logs case report forms and regulatory documents
- 4Schedule volunteers for appointments procedures and inpatient stays
- 5Assess volunteer eligibility through interviews and medical record reviews
- 6Communicate with laboratories investigators and nursing staff about procedures
- 7Educate volunteers on study protocols diary completion and device usage
- 8Coordinate site visits and communicate with sponsors CROs and investigators
- 9Prepare source documentation and collaborate with QA on protocol changes
- 10Record adverse events and discuss reporting with investigators
- 11Track enrollment status in Clinical Conductor system
- 12Perform protocol-specific tasks like interviewing volunteers and taking vital signs
- 13Participate in quality assurance audits and ship laboratory specimens
Requirements5
- 1BS/BA in Life Science or related discipline minimum 3 years clinical trial coordination experience
- 2Previous nursing medical assistant experience preferred
- 3CCRC certification
- 4Bilingual Spanish English fluency
- 5Strong communication and interpersonal skills
Salary Insight
$56 - $67k per year
Location
Required Skills
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