CRA I/CRA II/Sr CRA
Core
Conduct remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, manage documentation, and guarantee subject rights and data reliability for pharmaceutical and biotech clinical trials.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data and compliance reports for pharmaceutical and biotech sponsors
Domain
Life Sciences / Clinical Research
Required skills
Risk-based monitoring, root cause analysis, critical thinking, problem-solving, data accuracy verification (SDR/SDV/CRF), physical inventory management, ICH-GCP knowledge, regulatory compliance, site initiation, trial close-out, administrative reporting
Preferred skills
Medical/therapeutic area knowledge, Microsoft Office proficiency, ability to learn specialized software
Technologies
Clinical Trial Management Systems (CTMS), Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document review; manage investigator payments and site initiation; conduct trial close-out and material retrieval; prepare status reports; facilitate communication between sites, clients, and internal teams; maintain essential study documents.
Seniority
Entry to Mid-level, hands-on IC
