Clinical Research Associate jobs in United States
info-icon
This job has closed.
company-logo

Dexian · 4 hours ago

Clinical Research Associate

Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. They are seeking a Clinical Research Associate to monitor clinical research studies, ensure protocol compliance, and manage trial master file documentation.

ConsultingHuman ResourcesInformation TechnologyProfessional ServicesStaffing Agency
check
H1B Sponsor Likelynote
Hiring Manager
Prathamesh Waghmode
linkedin

Responsibilities

Direct experience monitoring clinical research studies
Site qualification, initiation, monitoring, and close-out visits (SQV/SIV/IMV/COV)
Ability to ensure protocol compliance, data integrity, and audit readiness
Experience working under SOPs and applicable regulations
Willing and able to travel up to 60% (domestic; international is a plus)
Able to independently manage travel logistics
Site training on protocol, CRFs, and source documentation
Ongoing site support and issue resolution
Real-time filing and maintenance of Trial Master File documentation
Understanding of inspection-ready TMF practices
Accurate source data verification
CRF review and report validation support

Qualification

Clinical MonitoringICH-GCP KnowledgeTMF ManagementSite TrainingDocumentation Skills

Required

Minimum 3+ years of hands-on CRA / Clinical Monitoring experience
Direct experience monitoring clinical research studies
Site qualification, initiation, monitoring, and close-out visits (SQV/SIV/IMV/COV)
Strong knowledge of ICH-GCP and regulatory requirements
Ability to ensure protocol compliance, data integrity, and audit readiness
Experience working under SOPs and applicable regulations
On-site monitoring experience with travel flexibility
Willing and able to travel up to 60% (domestic; international is a plus)
Able to independently manage travel logistics
Experience working directly with clinical trial sites
Site training on protocol, CRFs, and source documentation
Ongoing site support and issue resolution
TMF management experience
Real-time filing and maintenance of Trial Master File documentation
Understanding of inspection-ready TMF practices
Bachelor's degree (BS or BA) or equivalent experience
Life sciences preferred, but degree itself is required
Strong documentation and data review skills
Accurate source data verification
CRF review and report validation support

Company

Dexian provides services for staffing, talent development, and consulting, with a focus on technology, finance, and project management.

H1B Sponsorship

Dexian has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (65)

Funding

Current Stage
Late Stage

Leadership Team

leader-logo
Mahfuz Ahmed
Chairman of the Board
linkedin
leader-logo
Vikram Motiani
Managing Director
linkedin
Company data provided by crunchbase