Clinical Research Associate II, Phase I - Texas/Mid-West at Fortrea Topeka, KS

Clinical Research Associate II, Phase I - Texas/Mid-West Job at Fortrea, Topeka, KS
Fortrea seeks a Clinical Research Associate II with Phase I experience to monitor clinical trial sites across Texas and the Mid-West. The role involves site management, protocol compliance verification, data integrity oversight, and serious adverse event reporting with 40-50% travel required.
Monitor clinical sites including routine site visits, file maintenance, and protocol initiation
Review case report forms for data integrity and generate queries against data management systems
Complete and coordinate serious adverse event reporting and follow-up
Act as local project coordinator and client contact as assigned

University or college degree or certification in allied health profession
1+ years of clinical monitoring experience
Willingness to travel 40-50% overnight
Proficiency with electronic data collection systems
Ability to work in fast-paced, changing priority environment

Local area, Night shift
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