Clinical Trial Associate
Core
Supporting day-to-day clinical trial operations across multiple studies to ensure smooth execution and compliance.
Role type
Clinical Trial Associate
Builds
Clinical trial studies for ophthalmic therapeutics
Domain
Biotechnology / Ophthalmology / Clinical Research
Deliverable
client delivery
Required skills
GCP and ICH guidelines knowledge, budget management, invoice review and approval, vendor coordination, data tracking, user access management, documentation maintenance
Preferred skills
Experience in biotech/pharma/CRO, proficiency in Microsoft Excel, ability to learn new systems quickly
Technologies
Microsoft Excel, electronic study platforms, Trial Master File (TMF) systems
Responsibilities
Finalize and maintain site budgets, review and approve site invoices, coordinate vendor payments, maintain study trackers, generate enrollment and performance reports, manage user access across study systems, prepare meeting minutes and study documentation, support TMF maintenance
Seniority
Mid-level, hands-on IC
