Senior Clinical Research Associate II - Remote, High Travel

Actalent; United States; Remote; USD 87,000 - 89,000; Full time

Benefits offered by this job

All travel hours paid

Benefits provided

Job summary

Actalent seeks a Senior Clinical Research Associate II for a 6-month renewable contract. The role involves coordinating clinical monitoring and site management across diverse studies, with remote and on-site visits, and travel that covers door-to-door logistics.

You will ensure adherence to ICH-GCP, manage essential documentation, and perform SDR/SDV reviews to maintain data integrity. This home-based role requires strong collaboration with sponsors and sites.

Qualifications

• Bachelors degree in a life sciences-related field.
• 2+ years of independent clinical monitoring experience.
• Valid driver’s license where travel is required.
• Experience with on-site and remote monitoring activities.
• Strong understanding of ICH-GCP guidelines and related regulations.
• Excellent written and spoken English communication.

Responsibilities

• Perform and coordinate all aspects of clinical monitoring and site management.
• Conduct remote and on-site monitoring visits using a risk-based approach.
• Identify site process failures and implement corrective actions.
• Review SDR/SDV and CRFs to ensure data integrity.
• Manage investigational product accountability and site documentation.
• Prepare clear monitoring reports and follow-up letters.

Skills

Bachelors degree life sciences

Registered Nursing

Valid driver license

On-site & remote monitoring

ICH-GCP knowledge

English proficiency

Communication skills

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 a 6-month renewable contract. The role involves coordinating clinical monitoring and site management across diverse studies, with remote and on-site visits, and travel that covers door-to-door logistics.

You will ensure adherence to ICH-GCP, manage essential documentation, and perform SDR/SDV reviews to maintain data integrity. This home-based role requires strong collaboration with sponsors and sites.