Clinical Trial Management Specialist

Job Summary

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