Monitor and own the progress of clinical studies at investigative sites
Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
Coordinate all necessary activities required to set up and monitor a study
Work with 2-3 protocols on average and support Project Managers with larger scope trials
Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations

Requirements

4-year college degree or equivalent experience
2+ years CRA experience within the CRO or pharmaceutical industry to be considered for a CRA II
4+ year of CRA experience within the CRO or pharmaceutical industry to be considered for a Sr. CRA
Experience in monitoring oncology
Availability for domestic travel including overnight stays, up to approximately 50-60% travel commitment
Fluency in English and for non-English speaking countries the local language of country where position based

Benefits

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

clinical study monitoringprotocol adherenceSOP complianceICH-GCPoncology monitoringproject management supportclient presentationspayment initiation

communicationorganizational skillsinterpersonal skills

4-year college degreeCRA certification