Senior Clinical Research Associate II — Remote, Travel-Paid

Actalent; Albuquerque (NM); Remote; USD 87,000 - 89,000; Full time

Benefits offered by this job

Medical

Dental & vision

Critical Illness

Accident

Hospital

401(k) Retirement Plan Pre-tax and R​◦

Life Insurance

Short and long-term disability

Health Spending Account

Transportation benefits

Employee Assistance Program

Time Off/Leave

Job summary

Actalent is hiring a Senior Clinical Research Associate II for a 6-month renewable contract, 100% home-based with travel. The role focuses on monitoring and site management across diverse studies, ensuring compliance with ICH-GCP and SOPs, and maintaining data integrity.

Travel is substantial, and benefits are provided. The position requires strong clinical monitoring experience, excellent communication, and proficiency with CTMS and Microsoft Office.

Qualifications

• Bachelors in a life sciences field or RN with relevant qualifications.
• 2+ years of independent clinical monitoring experience.
• Valid driver's license where travel is required.
• Experience with on-site and remote monitoring activities.

Responsibilities

• Perform and coordinate clinical monitoring and site management per protocols, ICH-GCP, regulations, and SOPs.
• Conduct remote and on-site visits using risk-based monitoring for protocol adherence and data quality.
• Identify site process gaps, perform root cause analyses, and implement corrective actions.
• Ensure data accuracy via SDR/SDV and CRF reviews during monitoring visits.
• Verify investigational product handling and storage documentation.

Skills

Clinical monitoring

Monitoring on-site/remote

ICH-GCP

Data integrity

Risk-based monitoring

Communication skills

Problem-solving

Team coordination

CTMS proficiency

English proficiency

Education

Bachelors in life sciences

RN certification

Tools

CTMS

Microsoft Office

Job description

Actalent is hiring a Senior Clinical Research Associate II for a 6-month renewable contract, 100% home-based with travel. The role focuses on monitoring and site management across diverse studies, ensuring compliance with ICH-GCP and SOPs, and maintaining data integrity.

Travel is substantial, and benefits are provided. The position requires strong clinical monitoring experience, excellent communication, and proficiency with CTMS and Microsoft Office.