FSP CRA I & CRA II - Respiratory & Cardiovascular - Southeast region
Core
Conduct remote or on-site clinical monitoring and site management to ensure trials comply with protocols, ICH-GCP guidelines, and regulations for Respiratory and Cardiovascular studies.
Role type
Clinical Research Associate (Level I & II)
Builds
Clinical trial data integrity and regulatory compliance
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical monitoring, ICH-GCP knowledge, Risk Based Monitoring, Root cause analysis, Medical terminology, Microsoft Office
Preferred skills
Respiratory (COPD, asthma) and Cardiovascular therapeutic area knowledge
Technologies
Microsoft Office
Responsibilities
Conduct remote or on-site visits to assess protocol and regulatory compliance, manage required documentation, ensure audit readiness, develop collaborative relationships with investigational sites
Seniority
Entry to Mid-level, hands-on IC