[Hiring] Clinical Research Auditor I @NMDP

Role Description

This role ensures compliance with the NMDP/CIBMTR Research Database Protocol by conducting audits at Transplant and Cellular Therapy Centers. It demands strong professional judgment, real-time decision-making, and the ability to interpret and apply complex data reporting guidelines. The position involves performing data validation audits that include:

• Comparing source documents to NMDP registry data
• Identifying discrepancies
• Ensuring accurate reporting

The auditor analyzes findings to detect patterns, generate actionable insights, and develop clear, concise follow-up reports that drive corrective actions. Additionally, the role requires building and maintaining collaborative relationships with center staff, effectively communicating technical guidance, and promoting a shared commitment to data quality and continuous improvement.

Qualifications

• Knowledge of clinical research study processes, study design and/or protocol management.
• Knowledge of medical terminology and anatomy/physiology.
• Proficiency in Microsoft Suite of software products.
• Training and conflict resolution skills.

Requirements

• Execute responsibilities with a high level of attention to detail, ensuring accuracy and consistency across complex tasks.
• Communicate clearly and professionally with staff and site personnel, both verbally and in writing.
• Independently manage multiple, competing deadlines and priorities.
• Operate effectively in a remote work environment, demonstrating strong self-motivation, time management, and accountability.
• Travel approximately 35-50%, both domestic and international, depending on audit schedule.
• Bachelor’s degree in healthcare/science related field, or equivalent related experience and/or education.
• Minimum one year experience monitoring clinical research studies and/or protocol management.
• On evaluation, one year of previous experience in a Senior Clinical Data Analyst, Clinical Research Coordinator III, or equivalent position may be substituted for the experience requirement.

Preferred Qualifications

• Knowledge of blood and marrow transplant clinical research and medical field.
• ACRP or SOCRA certification.

Benefits

• Medical, dental, vision, life and disability insurance.
• Accident/critical illness/hospital benefits.
• Well-being, legal, identity theft, and pet benefits.
• Retirement plans.
• Paid time off/holidays.
• Leave and incentive plans for eligible employees.