Clinical Project Specialist

Job Summary

Providing project management and administrative support for clinical studies, the full-time Clinical Project Specialist will assist with document management, ensure compliance with regulatory requirements, and coordinate study-related activities in a hybrid work environment.

Key responsibilities

• Perform administrative and project support activities related to clinical trial execution, including document development and reconciliation
• Support day-to-day operations of clinical studies in compliance with applicable SOPs and regulatory guidelines
• Track and maintain study-specific information using various tools, and coordinate meetings and documentation for study teams

Required qualifications

• Preferred Bachelor's degree or equivalent relevant experience
• 2+ years of experience in the pharmaceutical, biotechnology, CRO, or clinical research environment
• At least 1 year of experience in a clinical operations support role such as Clinical Project Specialist or Clinical Trial Assistant
• Experience with clinical trial systems like CTMS, eTMF, or EDC is preferred
• Strong organizational skills with the ability to manage multiple priorities and deadlines