Experienced Clinical Research Associate (Level I/II) - FSP - Multi Therapeutics - Central US
Core
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical sponsors.
Role type
Clinical Research Associate (Level I/II)
Builds
Clinical trial execution and site management for pharmaceutical sponsors
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical monitoring, Risk Based Monitoring (RBM), Root Cause Analysis (RCA), ICH-GCP compliance, Site initiation and close-out, Data review (SDR/SDV/CRF), Investigational product inventory
Preferred skills
Medical/therapeutic area knowledge, Critical thinking, Problem-solving, Microsoft Office proficiency
Technologies
Clinical Trial Management Systems (CTMS)
Responsibilities
Monitor investigator sites using risk-based approaches to identify and resolve compliance issues; Conduct on-site and remote monitoring activities including data and inventory reviews; Initiate and close out clinical trial sites; Facilitate communication between sites, sponsors, and project teams; Respond to audits and inspections; Maintain essential study documents and track trial progress.
Seniority
Entry to Mid-level, hands-on IC