Clinical Trials Project Manager

Job Summary

A company is looking for a Project Manager - Startup & Feasibility.

Key Responsibilities

• Manage initial study submissions and serve as a liaison to sponsors and external IRBs
• Collaborate with investigators and Clinical Trials Support Services for budget development and regulatory submissions
• Support timely study start processes and mentor regulatory coordinators

Required Qualifications

• Bachelor's degree
• Minimum of 2 years of experience in regulatory management of oncology clinical trials in an academic setting
• Working knowledge of clinical trials and relevant Federal, State, and Local Regulations
• Familiarity with IRB requirements, consent form, and protocol development