Regulatory Project Manager

A company is looking for a Regulatory Project Manager, Hematology / Oncology (Fully Remote).

Key Responsibilities

Coordinate regulatory aspects of complex clinical research studies

Prepare, manage, and submit all required study and regulatory documents

Collaborate with study monitors to ensure compliance with regulatory requirements

Required Qualifications

Minimum of 3+ years of clinical research coordination experience

Experience with budget and negotiation

Proficiency in Adobe and Microsoft Office, especially Excel

Knowledge of clinical research concepts and human safety regulations

Experience with various local and external IRBs and research committees