Research Compliance Specialist
2 days ago
This position will provide support to the Clara D. Bloomfield Center for Leukemia Outcomes Research.
Duties Included:
Maintaining research compliance for projects within the Bloomfield Center.
Coordinate regulatory processes for research protocols (e.g., IRB and other regulatory agencies).
Assist in the writing of research protocols and will be responsible for research protocol submissions (amendments, continuing reviews, etc.).
Responsible for maintaining records for research protocols, ensuring protocol compliance and preparing for regulatory audits.
Serve as the point of contact for the Outcomes Research Consortium and Myeloid Disorder Registry and will coordinate data entry for the consortium databases.
Responsible for submitting Data Use Agreement requests and following up with collaborating centers for the completion of all protocol compliance and data submission questions.
Collect and analyze data to support research protocols.
Assist in data entry and quality control of REDCap databases.
Help to manage complex data sets, ensure the validity and integrity of data, maintain records and generate reports for process improvement and data reporting.
Assist in research collaborations, supervising research databases, managing data quality and participate in meetings.
Education and Experience:
A Bachelors degree in an appropriate field or an equivalent combination of education and experience is required.
2 years of relevant experience is preferred.
Successful completion of a background check is required; qualified candidates may be asked to complete a pre-employment physical including a drug screen.
Please provide three to five references
Function: Research Administration
Subfunction: Research Compliance
Band: Individual Contributor - Specialized
Level: S1 - Entry
Pay range: $24.52 - $32.21 hourly
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