Remote Senior Clinical Research Associate (SCRA) – Freelance

ProPharma Group; Greater London; Hybrid; GBP 65,000 - 101,000; Full time

Job summary

ProPharma Group is seeking a Freelance Senior Clinical Research Associate to support UK & Ireland studies. You will monitor sites, ensure GCP and SOP compliance, and collaborate with project teams.

Responsibilities include initiation, interim and close-out visits, site training, data accuracy checks, and coordination of supplies, with remote and on-site options in a hybrid, globally compliant setup.

Qualifications

• Bachelor's degree or equivalent
• 5+ years of experience as a Clinical Research Associate
• Experience with EDC, CTMS, IVRS and eTMF
• Knowledge of GCP, ICH guidelines and local/regulatory requirements

Responsibilities

• Conduct monitoring visits and co-monitoring, including initiation, interim and close-out visits
• Prepare monitoring reports per SOP and regulatory requirements
• Support site start-up activities and essential documents collection (Ex-US)
• Develop study-specific documentation and site tools
• Manage site training and data source documentation compliance
• Review source documents and CRFs for accuracy and data integrity
• Coordinate supply management and inventory of investigational products
• Communicate with sites, investigators and cross-functional teams
• Participate in meetings with project teams

Skills

Clinical monitoring

Regulatory knowledge

Communication

Organization

Remote work

Education

Bachelor's degree

Tools

EDC

CTMS

IVRS

eTMF

Job description

ProPharma Group is seeking a Freelance Senior Clinical Research Associate to support UK & Ireland studies. You will monitor sites, ensure GCP and SOP compliance, and collaborate with project teams.

Responsibilities include initiation, interim and close-out visits, site training, data accuracy checks, and coordination of supplies, with remote and on-site options in a hybrid, globally compliant setup.