CRA (Level II)
Core
Conducts remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, guaranteeing subject rights and data reliability.
Role type
Clinical Research Associate (Level II)
Builds
Clinical trials for life sciences and pharmaceutical clients
Domain
Life Sciences / Clinical Research
Deliverable
client delivery
Required skills
Clinical monitoring, ICH-GCP guidelines, risk-based monitoring, root cause analysis, data review (SDR/SDV/CRF), site initiation, trial close out, regulatory compliance
Preferred skills
Medical/therapeutic area knowledge, problem-solving, digital literacy
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; initiate and close out clinical trial sites; conduct on-site file reviews; track trial status and update study systems; respond to audits and inspections; manage investigator payments.
Seniority
Entry-level to Junior, hands-on IC