Senior Clinical Research Associate - Remote

Overview

The Senior Clinical Research Associate is responsible for ensuring compliance and performance for clinical research protocols and sites, acting as the primary contact throughout the study phases while developing site relationships and managing site activities.

In Short

• Accountable for site management and compliance with protocols.
• Acts as primary site contact throughout clinical trials.
• Develops and expands clinical research territory.
• Performs on-site and remote monitoring activities.
• Ensures data integrity and subject safety.
• Coordinates tasks with sponsor roles for site readiness.
• Identifies and resolves site performance issues.
• Mentors junior CRAs and participates in training.
• Supports audit and inspection activities.
• Travel required approximately 65-75% of working time.

Requirements

• Associate Degree or equivalent in a scientific/healthcare discipline.
• 7 years of relevant healthcare experience, including 4 years in site management.
• Bachelor's Degree preferred with direct monitoring experience.
• Relevant therapeutic experience is a plus.
• Ability to travel domestically and internationally.

Benefits

• Flexible work arrangements.
• Opportunity to work with a global healthcare leader.
• Participation in a diverse portfolio of research.
• Mentorship opportunities.
• Continuous training and improvement initiatives.