California Licensed Project Manager

Job Summary

Providing project management support for investigator-initiated clinical trials, the full-time Sr. Project Manager will oversee study documentation, regulatory submissions, and data quality while working remotely from Los Angeles, CA.

Key responsibilities:

• Serve as the primary point of contact for investigators and study teams, ensuring effective communication and oversight of clinical research studies
• Write and manage protocols and regulatory submissions, including FDA IND and IRB documents, ensuring accuracy and timeliness
• Review study data and collaborate with teams to maintain data quality and compliance with research requirements

Required qualifications:

• Experience in clinical research project management
• Knowledge of clinical research protocols and regulatory processes
• Familiarity with Investigator Initiated Trials (IITs) is preferred