Assoc CRA • Monitoring
Core
Conduct clinical monitoring visits for research studies under close supervision, ensuring adherence to protocols and regulations.
Role type
Associate Clinical Research Associate (Monitoring)
Builds
Clinical trial data integrity and regulatory compliance for life sciences studies
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Clinical monitoring, GCP/ICH guidelines, protocol adherence, site management, regulatory submissions tracking, CRF management, data query resolution, documentation management, site recruitment support
Preferred skills
Prior clinical experience, scientific or healthcare degree, therapeutic/protocol training
Technologies
Microsoft Word, Excel, PowerPoint, laptop, iPhone, iPad
Responsibilities
Perform site monitoring visits (selection, initiation, monitoring, close out), administer protocol training to sites, evaluate site practice quality, track regulatory submissions and enrollment, manage CRF completion and data queries, maintain TMF and ISF documentation, support start-up phase, generate visit reports and action plans, assist in subject recruitment planning
Seniority
Entry-level, supervised IC