Senior CRA II | Remote Contract, 60-80% Travel

Actalent; Houston (TX); Remote; USD 87,000 - 90,000; Full time

Benefits offered by this job

Travel paid

Benefits provided

Job summary

Actalent seeks a Senior Clinical Research Associate II for contract-based work supporting diverse studies across sponsors. The role combines remote and on-site monitoring with travel, following ICH-GCP guidelines and SOPs.

Responsibilities include monitoring visits, data quality, site management, and collaboration with cross-functional teams to ensure regulatory compliance and patient safety.

Qualifications

• Bachelor's degree or nursing qualification required with life sciences focus.
• Minimum 2+ years of independent clinical monitoring experience.
• Valid driver's license where travel is required.
• Proven knowledge of ICH-GCP and regulatory guidelines.

Responsibilities

• Perform and coordinate clinical monitoring and site management.
• Conduct remote and on-site visits using risk-based monitoring.
• Identify site process issues and implement corrective actions.
• Ensure data accuracy through SDR/SDV and CRF review.
• Monitor investigational product accountability and records.
• Prepare clear monitoring reports and follow-up letters.

Skills

Clinical monitoring

Site management

Risk-based monitoring

Data integrity

ICH-GCP guidelines

Regulatory compliance

Documentation

Communication skills

Travel willingness

Problem solving

Education

Bachelor's degree in life sciences

Registered Nursing certification

Tools

CTMS

Microsoft Office

Job description

Actalent seeks a Senior Clinical Research Associate II for contract-based work supporting diverse studies across sponsors. The role combines remote and on-site monitoring with travel, following ICH-GCP guidelines and SOPs.

Responsibilities include monitoring visits, data quality, site management, and collaboration with cross-functional teams to ensure regulatory compliance and patient safety.