Compliance Officers

Moffitt Cancer Center · Remote, United States

To support research regulatory activities through the critical evaluation and completion of protocol specific documents and standardized reports for effective and compliant protocol activity from activation through closure. The primary focus is on regulatory document completion, submission, proper filing and reporting to achieve and maintain compliance with internal policies, external sponsor, state statutes, and federal regulations pertinent to research involving human subjects.
Independently prioritizes and critically evaluates the specific regulatory requirements and submissions for each study in assigned program(s).
~ Identify the difference between compassionate use, emergent use, humanitarian device, biomedical, and social science studies to file the appropriate IRB application.

~ Create, maintain and update informed consent forms and IRB/IBC Applications.
~ Review and extract all required data from the protocol, investigators brochure, and any other pertinent source documentation to complete the application process to include drafting the informed consent by combining model consent language with Institutional and respective IRBs terminology.

~ Independently process applications for Biosafety Committee review in conjunction with IRB applications.

Mentoring and Training of new regulatory staff.
~ Provides mentoring/training to new regulatory staff as well as other members of the research team(s).

Act as central contact for regulatory queries, providing documentation and processing requests.
~ Serves as the primary liaison for protocol regulatory support and will be in constant communication with internal and external customers; Gather required documentation for internal/external audits collaborating with the research staff and draft regulatory responses.

Regulatory Files Creation and Maintenance
~ Assist in assuring that all study documents, including SOPs and regulatory files are maintained in audit-ready condition.

High School Diploma/GED required.

~ HSD with 4 or more years of clinical research regulatory experience (preferably in oncology).

~ Associates or Bachelors Degree with 2 years of clinical research regulatory experience (preferably in oncology).

~ Masters Degree with 1 year of clinical research regulatory experience (preferably in oncology).

Two (2) years experience in clinical research regulatory experience, including study activation.

~ Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.
Moffitt Career Site

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.
Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at or by email at contact information is for accommodation requests only and cannot be used to inquire about the status of applications.
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