FSP CRA I
Core
Conducts remote or on-site clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulations.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial operations for a functional service provider (FSP)
Domain
Clinical research / Healthcare
Deliverable
client delivery
Required skills
Clinical monitoring, Site management, ICH-GCP compliance, Risk Based Monitoring, Medical terminology, Root cause analysis, Microsoft Office
Preferred skills
Life sciences background, Registered Nursing certification, English language proficiency
Responsibilities
Conduct remote or on-site visits to assess protocol and regulatory compliance, Manage required documentation, Develop collaborative relationships with investigational sites, Ensure audit readiness
Seniority
Entry-level to Mid-level
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