Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available
Core
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical clinical trials.
Role type
Senior Clinical Research Associate (CRA II)
Builds
Clinical trial data integrity and regulatory compliance for sponsors in multiple therapeutic areas
Domain
Life Sciences / Clinical Research / Pharmaceutical Trials
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, protocol compliance, ICH-GCP guidelines, site management, data verification (SDR/SDV), investigator site identification, trial close-out
Preferred skills
Therapeutic area knowledge (Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, Pulmonary), critical thinking, problem-solving
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches; ensure data accuracy through document and record review; assess investigational product inventory; escalate and resolve site deficiencies; initiate and close out clinical trial sites; provide trial status tracking reports; respond to regulatory audits and inspections.
Seniority
Mid-level, hands-on IC
