Sr. Project Manager

Avispa Technology • Los Angeles, CA

16h • Remote

About The Position

A leading medical institution is seeking a Sr. Project Manager to provide project management support and oversight for investigator-initiated clinical trials within a hematology/oncology clinical research team. The role works under the direction of investigators and clinical research unit leadership and serves as the primary point of contact for investigators, regulatory and study coordinators, data managers, research staff, and study monitors. The position is remote and is a three-month assignment at 40 hours per week.

Requirements

• Experience or demonstrated ability in clinical research project management.
• Knowledge of clinical research protocols, study documentation, and regulatory processes, including FDA IND, DSMB, and IRB submissions.

Nice To Haves

• Experience with Investigator Initiated Trials (IITs).

Responsibilities

• Provide project management support and oversight for assigned investigator-initiated clinical research studies.
• Serve as the primary point of contact for investigators, regulatory and study coordinators, data managers, research staff, and study monitors.
• Write protocols and study documents accurately and on time.
• Help prepare and complete FDA IND, DSMB, IRB, and other regulatory submissions.
• Review and follow up on study data and monitoring findings, collaborating with study teams and study monitors to support data quality.
• Maintain regulatory files and ensure study documentation is complete, accurate, and current to meet research requirements and established study timelines.
• Manage assignments from the team director and study investigators, adjusting priorities based on study and departmental needs.
• Ensure study and patient care needs are addressed appropriately and on time.

Benefits

• Group medical, dental, vision, and life coverage.
• Retirement Savings Program.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed