Clinical Trial Management Specialist

A company is looking for a Clinical Trial Management Support Specialist (Contractor).

Key Responsibilities

Manage support requests by routing, updating, and resolving CTMS-related inquiries

Data entry and maintenance of Drug Program and Investigator data within the CTMS

Conduct data quality activities, including internal audits to eliminate duplicates

Required Qualifications

High School Diploma or international equivalent, preferably in a technical, clinical, or health-related field

0 to 3 years of experience with clinical trial management systems or managing clinical trial data

Familiarity with drug development and clinical trial processes preferred

Proven ability to ensure a successful customer experience through quality deliverables

Strong analytical and organizational skills, capable of managing multiple projects in a fast-paced environment