Senior Clinical Research Associate - Remote Contract

Actalent; United States; Remote; USD 81,000 - 86,000; Full time

Job summary

Actalent is seeking a Senior Clinical Research Associate I (Sr CRA I) for a 6-month contract based out of Houston, TX. The role is 100% remote with substantial travel (60–80%), and offers W2 benefits.

You will perform remote and on-site monitoring, ensure ICH-GCP compliance, and manage trial data across multiple sponsor models in a global clinical research setting. Responsibilities include monitoring patients and sites, data integrity, regulatory adherence, and collaboration with project teams

Qualifications

• ,

Responsibilities

• Perform remote and on-site clinical monitoring and site management for trials.
• Monitor sites using risk-based monitoring; identify issues; implement corrective actions.
• Ensure data accuracy through SDR/SDV and CRF review.
• Maintain audit readiness and timely monitoring reports.
• Escalate deficiencies and drive resolution with project teams.
• Support trial status tracking and CTMS/data systems updates.
• Participate in investigator meetings and site training.
• Initiate sites per procedures and ensure regulatory compliance.

Skills

Clinical monitoring

On-site monitoring

Remote monitoring

ICH-GCP

Regulatory compliance

Data integrity

Communication

Team collaboration

Problem solving

English proficiency

Education

Bachelor's degree in life sciences or RN certification

Tools

CTMS

Microsoft Office

EDC

Job description

Actalent is seeking a Senior Clinical Research Associate I (Sr CRA I) for a 6-month contract based out of Houston, TX. The role is 100% remote with substantial travel (60–80%), and offers W2 benefits.

You will perform remote and on-site monitoring, ensure ICH-GCP compliance, and manage trial data across multiple sponsor models in a global clinical research setting. Responsibilities include monitoring patients and sites, data integrity, regulatory adherence, and collaboration with project teams