Regulatory Compliance Officer-NE

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Job Title:
Regulatory Compliance Officer-NE

Department:
CCC | Clinical Trials Office

The Regulatory Compliance Officer assures that research protocols of the OSUCCC Clinical Trials Office (CTO) are in compliance with University, state and federal regulations; ensures timely submission of all appropriate paperwork for review by appropriate agency.

Responsibilities:

• Collaborates with investigators during study development to facilitate and confirm that appropriate regulatory safeguards have been included
• Conducts detailed reviews of assigned protocols and informed consent forms prior to IRB review
• Ensures timely submission of protocol documents for review by appropriate agency communicates with all CTO research projects sponsors (academic, federal, industry) to ensure compliance
• Interfaces with various internal and external entities to coordinate and effectively compile all appropriate data relevant to the conduct of a CTO trial
• Develops IRB submission packets for protocols, including writing of abstract, submission of standard forms and drafting of informed consent forms
• Provides and maintains tracking system to assess progress of a protocol's review; maintains regulatory essential files on submitted and approved studies
• Reviews all protocol revisions and amendments; amends consent forms if needed and follows established guidelines to determine if amendments requires IRB review
• Distributes all amendments and IRB approved informed consent forms to relevant university protocol holders
• Acts as main point of contact for the dissemination of all approved study material and works collaboratively with various internal and external departments to ensure relevant updates are communicated effectively and timely
• Attends meetings; serves as principal contact from CTO to regulatory agencies including FDA and IRBs
• Continually monitors federal and sponsor rules, regulations and processes to identify and interpret new, updated or changed requirements
• Provides regulatory updates and guidance to investigators and research staff of new or changed regulations; participates in audits and site visits

Minimum Education Requirements:

Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required; 1 year experience in research or administrative capacity working on research projects; knowledge of research regulations, guidelines and compliance issues required; experience developing informed consent documents and preparing regulatory documents desired; experience and knowledge of IRB and federal or industry sponsor processes and requirements preferred. Requires successful completion of a background check. Selected candidate may be requested to complete a preemployment physical including a drug screen.

Salary Range for this position: $20.25 - $30.38 hourly

Additional Information:

The OSUCCC – James is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nation‐ally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nation’s largest public universities.

Location:
Remote Location

Position Type:
Regular

Scheduled Hours:
40

Shift:
First Shift

Final candidates are subject to successful completion of a background check.  A drug screen or physical may be required during the post offer process.

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