Senior Clinical Research Associate
Washington, Connecticut, United States of America
Full Time
13 hours ago
No Visa Sponsorship
Key skills
Google Cloud PlatformGCPGoogle CloudResource PlanningCommunication
About this role
Role Overview
- Perform on-site and remote monitoring visits to ensure subject safety and data quality
- Review CRFs and source documentation for accuracy and completeness
- Ensure informed consent procedures and protocol compliance are met
- Manage and track Investigational Product accountability
- Prepare monitoring visit reports and follow up on action items
- Maintain and update eTMF, CTMS, and trial documentation systems
- Support sites with issue resolution and ensure timely completion of deliverables
- Participate in audits and inspections, including preparation and follow-up
- Collaborate with project teams and contribute to monitoring plans, project tracking, and CRA resource planning
Requirements
- Bachelor’s degree in Life Sciences, Nursing, or equivalent
- Minimum 3+ years of CRA experience, including on-site monitoring
- Strong understanding of GCP, ICH, and regulatory requirements
- Experience working in a fast-paced, matrix organization
- Excellent communication and organizational skills
- Fluent in English
- Strong attention to detail and problem-solving mindset
- Ability to work independently and collaboratively
- Experience in dermatology is considered a strong advantage.
Tech Stack
- Google Cloud Platform
Benefits
- Competitive compensation package
- Comprehensive benefits
- Opportunity for personal and professional growth
- Supportive work environment