Senior Clinical Trial Associate

Role: Clinical Trial Associate supporting the execution and management of ophthalmology clinical studies, under supervision. Responsibilities include assisting with study planning, protocol and documentation development, IRB submissions, site communication, monitoring support, and TMF maintenance. Ensures compliance with GCP, FDA, and international regulations across clinical investigations. Collaborates with cross-functional teams such as R&D, Regulatory, Safety, and Quality. Provides operational support, tracks study payments, and aids in study start-up activities. Qualifications: Bachelor’s in health or science field; minimum 3 years of clinical trial experience; strong knowledge of GCP and FDA regulations; proficient in medical terminology, communication, and computer skills. Preferred: advanced degree. Work setup is remote in the US, with minimal travel expected.