Experienced Clinical Research Associate (CRA II/Sr CRA) - AR, KS, LA, MO, OK, TX - Multiple Therapeutic Areas Available
Core
Conduct remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, manage documentation, and guarantee data reliability for pharmaceutical clinical trials.
Role type
Senior Clinical Research Associate (CRA II)
Builds
Clinical trial data and compliance reports for pharmaceutical sponsors
Domain
Life Sciences / Clinical Research
Required skills
Risk-based monitoring, Root cause analysis, Protocol compliance, ICH-GCP guidelines, Site initiation, Data review (SDR/SDV/CRF), Investigational product inventory, Audit readiness, Travel management
Preferred skills
Medical/therapeutic area knowledge, Clinical Trial Management Systems, Presentation skills
Technologies
Microsoft Office, Clinical Trial Management Systems
Responsibilities
Monitor investigator sites using risk-based approaches; Conduct on-site and remote monitoring activities; Initiate and close out clinical trial sites; Ensure essential documents are complete and compliant; Provide trial status tracking and progress reports; Facilitate communication between sites, clients, and project teams; Respond to regulatory audits and inspections.
Seniority
Senior, hands-on IC