Clinical Research Auditor I

🕒 June 18

❄️ Minnesota – Remote

❄️ Minnesota – Remote

⏰ Full Time

🟢 Junior

🧪 Clinical Research

👻 Ghost score 44%

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NMDP

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1987

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

NMDP is a nonprofit organization (formerly Be The Match) that operates the national blood stem cell donor registry and coordinates cell therapy to treat blood cancers and other blood disorders. It recruits and registers donors, matches donors to patients, facilitates transplants, provides patient support and financial assistance, conducts and funds clinical research and trials, and leads advocacy and fundraising to expand access to life‑saving cell therapies.

📋 Description

• Ensure compliance with the NMDP/CIBMTR Research Database Protocol by independently conducting audits at Transplant and Cellular Therapy Centers • Work autonomously with center staff, interpret complex reporting guidelines, make real-time decisions, and assess data reporting compliance • Lead site audits focused on data verification and regulatory review • Identify, prioritize, and resolve data reporting issues with transplant center staff • Build relationships with transplant center staff through mentoring and professional guidance • Analyze patterns and root causes in audit findings • Synthesize trends into actionable insights and author follow-up reports supporting corrective and preventative strategies • Provide technically sound guidance and facilitate collaborative discussions with site teams • Assist in developing and testing electronic data capture (EDC) systems, clinical trial management systems (CTMS), and other applications • Plan, organize, and execute special projects with minimal supervision

🎯 Requirements

• Knowledge of clinical research study processes, study design and/or protocol management • Knowledge of medical terminology and anatomy/physiology • Knowledge of Microsoft Suite software products • Training and conflict resolution skills • High attention to detail and accuracy • Clear and professional verbal and written communication skills • Ability to interpret complex technical information and adapt messaging to varied audiences • Ability to independently manage multiple competing deadlines and priorities • Ability to work effectively in a remote environment with self-motivation, time management, and accountability • Willingness and ability to travel approximately 35–50% domestically and internationally, potentially up to 70% • Bachelor’s degree in a healthcare/science-related field, with equivalent related experience and/or education potentially substituted • Minimum one year of experience monitoring clinical research studies and/or protocol management according to GCDMP/ICH GCP/FDA guidelines, or verifying clinical data from medical records • One year of Senior Clinical Data Analyst, Clinical Research Coordinator III, or equivalent CIBMTR/NMDP experience may substitute for the experience requirement • ACRP or SOCRA certification preferred • Knowledge of blood and marrow transplant clinical research and the medical field preferred

🏖️ Benefits

• Medical, dental, vision, life and disability benefits • Accident, critical illness and hospital benefits • Well-being benefits • Legal benefits • Identity theft benefits • Pet benefits • Retirement plans • Paid time off and holidays • Leave plans • Incentive plans