Demo

Research Compliance Auditor

HMH HOSPITALS CORPORATION
Edison, NJ Full Time
POSTED ON 1/22/2025
AVAILABLE BEFORE 3/22/2025

Our team members are the heart of what makes us better.

 

At Hackensack Meridian Health we help our patients live better, healthier lives — and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It’s also about how we support one another and how we show up for our community.

 

Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change.

 

The Research Compliance Auditor is a key contributor to HMH’s Research Compliance Audit and Monitoring Program (RCAMP) which is responsible for post-approval review and auditing of Hackensack Meridian Health Research portfolio for compliance with applicable policies, regulations, and best practices. The Research Compliance Auditor is also responsible for identifying and developing resources to support research compliance including but not limited to providing guidance and education on all areas of research compliance. This includes: FDA regulated clinical trials, human subjects research, federally and industry sponsored research. The position requires excellent attention to detail, good communication, initiative, and the ability to effectively manage competing high priority tasks. The position will report to the Research Compliance Officer.

Qualifications:

Education, Knowledge, Skills and Abilities Required:

  • Bachelor’s degree from accredited college or university in a relevant area of study (e.g. physical sciences, public health, biomedical sciences.). 
  • Minimum of 7 or more years of relevant professional experience in research administration and/or conducting research at an institution of higher education and/or academic medical center. 
  • Experience working with research administration software solutions.
  • Basic understanding of research regulations and processes in at least one area of research compliance (e.g. human subjects research, clinical billing, FDA regulated research, sponsored research.)
  • Strong organization skills, ability to be proactive and ability to work both independently and as part of a team. 
  • Skilled in making decisions based on critical and analytical thinking, experience and professional judgment. 
  • Excellent written and verbal communication skills. Including confidence and comfortable with public speaking. 
  • Proficient computer skills that may include but are not limited to Microsoft Office and/or Google Suite platforms.

 

Education, Knowledge, Skills and Abilities Preferred

  • Relevant professional certifications (CIP, CHC, CHRC, CIPA, etc.)
  • 5 years of research audit experience

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