Study Start-Up Associate

Job Summary

Providing administrative support for regulatory submissions on international clinical trials, the full-time Study Start-Up Associate II will create project timelines, track essential documents, and coordinate with cross-functional teams while working remotely.

Key responsibilities

• Creates MS project files to establish study start-up timelines for each country
• Tracks and follows up on missing documents and prepares regulatory submission packages
• Coordinates with study team members to collect and track essential documents for site activation

Required qualifications

• Bachelor's Degree in a healthcare-related field required; Master's Degree preferred
• 1-3 years of experience in pharma and/or CRO, with 1-2 years in study start-up activities
• Strong knowledge of the clinical research process related to study start-up and medical terminology
• Proficiency in MS Project, Word, and Excel
• Excellent organizational and interpersonal skills with a positive attitude