Senior Clinical Research Associate - Contract Position
Core
Senior Clinical Research Associate conducting full-site lifecycle monitoring for clinical trials of investigational and approved products.
Role type
Senior Clinical Research Associate (Contract)
Builds
Clinical trial data integrity and regulatory compliance
Domain
Pharmaceutical/Biotechnology clinical research
Required skills
Clinical trial monitoring, ICH GCP, FDA regulations, protocol compliance, data integrity, investigational supply management, site qualification, adverse event tracking
Preferred skills
Mentoring junior CRAs, resolving complex study challenges
Technologies
Microsoft Word, Excel, PowerPoint
Responsibilities
Conduct site visits (qualification, initiation, interim, close-out), monitor trial compliance, train site personnel, manage investigational supplies, track enrollment and adverse events, review source data and CRFs, resolve data queries, maintain study files (via careerplan.io/jobs/6f6e38df-523d-4173-87ec-56626c6a520c-senior-clinical-research-associate-contract-position-at-jobgether)
Seniority
Senior, hands-on IC with mentorship responsibilities