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Responsibilities
- Conduct and document remote site contacts and activities per SOPs and study guidance
- Conduct and document onsite activities under supervision
- Perform remote data review of EDC, CTMS, RBM to ensure SOPs and GCP compliance
- Identify trends within and across study sites and escalate findings
- Review the site section of the TMF for accuracy, timeliness, and completeness
- Support CRA II, Sr CRA, and Lead CRA in day-to-day study management activities
- Remotely monitor and resolve queries from data management activities
- Coordinate clinical site communications and provide ongoing updates
- Support audit preparation and required follow-up actions
- Identify and recruit site investigators; coordinate trial materials and documentation
- Ensure SOPs are in place to optimize patient recruitment and provide guidance
Requirements
- College diploma/degree and 1-3 years related experience
- SoCRA, CCRA and/or ACRP certification/designation is an asset
- Self-motivated with strong communication skills and commitment to results
- Strong attention to detail and collaborative relationship skills
Benefits
- Home-based work
- Regular travel
