FSP - CRA I - South Africa
Core
Conduct remote or on-site clinical monitoring and site management to ensure trials comply with protocols, ICH-GCP guidelines, and regulations, guaranteeing subject rights and data reliability.
Role type
Clinical Research Associate (Level I)
Builds
Clinical trial data and compliance reports for pharmaceutical and biotech sponsors
Domain
Clinical Research / Life Sciences
Required skills
Clinical monitoring, ICH-GCP guidelines, protocol compliance, site management, risk-based monitoring, medical terminology, root cause analysis, Microsoft Office
Preferred skills
Respiratory or Cardiovascular therapeutic area knowledge, Registered Nursing certification
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-level (6 months minimum travel monitoring experience required)
