$120K - 180K a year
Oversee CRA performance, manage and coach CRAs, ensure compliance with monitoring and trial execution standards, and liaise with CPMs for clinical trial progress.
7+ years clinical research experience with leadership in monitoring clinical trials, deep knowledge of drug development regulations and standards, and a 4-year degree in a relevant healthcare field.
Description: • Oversight of CRA performance, development and coaching of CRA • Managing and addressing CRA performance targets per defined KPIs: delivery, productivity, and quality performance indicators • Monitoring and approving CRA travel and expense to ensure compliance to T&E policy • Ensures CRA monitoring competency gaps are identified and resolved through targeted coaching and training curricula • Liaise on ongoing basis with CPMs to ensure enrollment, data collection and data cleaning are executed by CRAs in a timely manner Requirements: • 4-year degree plus relevant, related healthcare experience • Minimum 7 years’ experience in clinical research -planning/executing and/or monitoring clinical trials • Field Monitoring experience • Leadership experience • Experience in project management and evidence of team leadership capabilities • Understanding of all aspects of clinical drug development with particular emphasis on monitoring and trial execution • Thorough understanding of the international aspects of drug development process, including expert knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities regulations, risk-based monitoring and Novartis standards Benefits: • health • life and disability benefits • 401(k) with company contribution and match • generous time off package including vacation, personal days, holidays and other leaves
This job posting was last updated on 10/12/2025