What are the responsibilities and job description for the Clinical Research Coordinator position at Discover International?
About the Role
We’re seeking an experienced Clinical Research Coordinator to join a leading research facility in Los Angeles. This role offers the chance to directly support groundbreaking clinical studies while working closely with investigators and cross-functional teams.
Requirements
Required:
- Minimum 5 years of clinical research experience
- 5 years of experience with IRB application procedures
- Experience with Phases I–IV and investigator-initiated trials
Preferred:
- Bachelor’s degree
- Experience within pharmaceutical, biotechnology, or CRO environments
Key Responsibilities
- Provide clinical research expertise in study design, implementation, and patient coordination
- Oversee assigned research infrastructure and ensure compliance with institutional policies
- Act as a departmental liaison, supporting investigator-initiated protocols and committee coordination
- Develop and manage case report forms, budgets, and protocol documentation
- Ensure proper documentation (consents, CRFs, SAEs, source data) in compliance with FDA, IRB, HIPAA, and institutional standards
- Prepare and submit IRB documentation; ensure timely reporting to sponsors and CROs
- Serve as a main point of contact for Principal Investigators and sponsor representatives
- Support audit readiness and assist with study initiation and monitoring visits
- Participate in quality assurance initiatives and performance improvement projects
