Experienced Clinical Research Associate (CRA II / SR CRA)- Bilingual - US Southeast region - Multiple Therapeutic Areas Available
Core
Conduct remote and on-site clinical monitoring visits to assess protocol and regulatory compliance, manage documentation, and ensure audit readiness for clinical trials.
Role type
Clinical Research Associate (Level II)
Builds
Clinical trial data and compliance for pharmaceutical and biotech sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical monitoring, ICH-GCP guidelines, protocol adherence, site management, risk-based monitoring, medical terminology, root cause analysis, Microsoft Office
Preferred skills
Therapeutic area knowledge (Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, Pulmonary), PPD Drug Development Fellowship completion
Technologies
Microsoft Office
Responsibilities
Conduct on-site and remote monitoring visits, manage required documentation, ensure trial compliance with approved protocols and regulations, develop collaborative relationships with investigational sites, ensure audit readiness
Seniority
Mid-level, hands-on IC