Senior Clinical Research Associate (East Coast based)
Core
Conducts on-site and remote monitoring visits (Pre-Study, Initiation, Interim, Close-Out) to ensure investigational sites are adequate for clinical study conduct.
Role type
Senior Clinical Research Associate
Builds
Clinical trial data integrity and regulatory compliance for biopharmaceutical clients
Domain
Clinical research / Biopharmaceuticals
Required skills
Phase 2/3 trial monitoring, complex trial experience (oncology/rare disease), site qualification, staff training, regulatory submission support, mentoring
Preferred skills
None stated
Technologies
None stated
Responsibilities
Perform on-site or remote monitoring visits; Identify and verify investigator qualifications and resources; Train investigational site staff; Support preparation of regulatory/EC submissions; Mentor new staff and perform co-monitoring visits
Seniority
Senior, hands-on IC