More jobs:
Compliance Monitoring Specialist; Oncology
Job in
Baltimore, Anne Arundel County, Maryland, 21276, USA
Listed on 2026-01-27
Listing for:
ARMA International
Full Time
position Listed on 2026-01-27
Job specializations:
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science
Job Description & How to Apply Below
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.
- 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
- Bachelor’s Degree in Life Sciences, Health Care or a related field.
- Certification in human subject's research.
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
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