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"Compliance Monitoring Specialist (Oncology)"

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Compliance Monitoring Specialist (Oncology)

Compliance Monitoring Specialist (Oncology)

Johns Hopkins University

We are seeking a Compliance Monitoring Specialist who will be responsible for conducting compliance monitoring reviews of clinical research trials in keeping with established policies and procedures.

Specific Duties & Responsibilities

  • Schedule compliance monitoring visits with research study staff.
  • Develop protocol specific forms.
  • Review research and medical records against clinical protocols for compliance.
  • Prepare written summary of compliance review results.
  • Meet with principal investigators and data support staff to review compliance results.
  • Follow-up on results, as necessary.
  • Maintain scheduling and review information in OnCore for all protocol reviews.
  • Help study staff to prepare for external audits.
  • Participate in unscheduled internal reviews and compliance monitoring reviews at affiliate institutions as needed.
  • Schedule compliance monitoring visits with research study staff to monitor data integrity studies.
  • Generate queries and conduct follow-up for non-compliance issues.
  • Generate monitoring summary reports and communicate these findings.
  • Provide support for monitored trials in the form of research into regulations and review of protocols and Case report templates for protocol staff.
  • Assist staff in developing corrective actions for compliance review observations when appropriate.
  • Assist in training new research staff regarding research compliance; may make presentations to support this effort.
  • Participate on subcommittees by reviewing new studies for quality assurance and general content, and coding new studies.
  • Prepare reviews of studies by various committees.
  • Attend and participate in monthly meetings.
  • Assist in the development and maintenance of SOPs for the research manual on assigned areas website as needed.
  • Perform periodic compliance reviews.
  • Other duties as assigned.

Minimum Qualifications

  • Bachelor’s Degree.
  • Three years of related experience with clinical trials/medical research.
  • Additional education may substitute for required experience and additional related experience may substitute for required education beyond high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula

Preferred Qualifications

  • Bachelor’s Degree in Life Sciences, Health Care or a related field.
  • Certification in human subject's research.

Additional Details

Classified Title: Compliance Monitoring Specialist
Role/Level/Range: ACRP/04/MC
Starting Salary Range: $48,000 - $84,100 Annually ($65,400 targeted; Commensurate w/exp.)
Employee group: Full Time
Schedule: Mon - Fri / 8a - 4:30p
FLSA Status: Exempt
Location: Hybrid/School of Medicine Campus
Department name: SOM Onc Clinical Research Office
Personnel area: School of Medicine

Posted: 16-Dec-25
Location: Baltimore, Maryland
Categories: Staff/Administrative
Internal Number: 119861-en_US 1

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