Clinical Study Operations Associate

Job Summary

To support innovative clinical development, the remote Clinical Study Operations Associate will manage study logistics, coordinate with cross-functional teams, and ensure compliance with regulatory requirements.

Key responsibilities

• Managing study logistics and timelines for clinical trials
• Coordinating with internal and external stakeholders to facilitate study operations
• Ensuring compliance with regulatory guidelines and company policies throughout the study lifecycle

Required qualifications

• Bachelor's degree in a relevant field or equivalent experience
• Experience in clinical study operations or project management
• Familiarity with regulatory requirements in clinical research
• Proficiency in data management and reporting tools
• Strong organizational skills and ability to manage multiple projects simultaneously