Senior Regulatory Affairs and Research Systems Manager - Pediatrics

Department

BSD PED - Clinical Trials Office
About the Department

In the Department of Pediatrics at the University of Chicago, we strive to provide the highest level of complex care for children from diagnosis and treatment to conducting research to find promising new therapies with a focus on teaching. We are committed to advancing the frontiers of knowledge, and the education and training of future clinical pediatricians, subspecialists, educators, clinical investigators and physician-scientists. The Department of Pediatrics is a dynamic, stimulating place to work, and because we are focused on growth and improved excellence, our staff have particularly challenging and rewarding roles.

The Pediatric Clinical Trials Office (Peds CTO) is an existing centralized support office that provides services and high-level guidance to individuals (faculty, investigators, research staff, and clinic coordinators from the University and Hospital) involved in human subjects research. The Peds CTO is responsible for establishing standards, operating procedures, policies and practices, implementing educational and training programs, developing communication tools, and managing the administrative functions that impact individuals involved in clinical research.   
Job Summary

The Senior Regulatory Affairs and Research Systems Manager functions as a leader in the Department’s dynamic clinical research program by managing regulatory and compliance functions for studies conducted in the Department of Pediatrics, overseeing Clinical Trial Management System functionality, and provide expertise in research study conduct. The Senior Regulatory Affairs and Research Systems Manager will have specialized knowledge of regulatory requirements for conducting human subjects research across local and central IRBs; will be responsible for management and oversight of regulatory processes for all Pediatric clinical research programs and projects; and will mentor, guide, and train staff using technical systems. The research projects involve multi-centered cooperative group studies, single-site studies, inter-group studies, grant application and funded studies, industry studies, and investigator-initiated studies. The Senior Regulatory Affairs and Research Systems Manager will be expected to participate in established and future research programs and will serve as the main contact for regulatory purposes requiring interaction with principal investigators, co-investigators, affiliate institutions, sponsoring agents, the Food and Drug Administration (FDA), the Institutional Review Board (IRB), and other regulatory bodies. This role will also be responsible for developing and implementing quality improvement initiatives within the Pediatric Clinical Trials Office. This role will also be the primary liaison with the Divisional Office of Clinical Research for Pediatric representation with Clinical Trial Management Systems.

Responsibilities

• Oversee Departmental Clinical Research Portfolio across the lifecycle for each protocol from feasibility, startup, recruitment, day-to-day conduct, follow up through study close out, including Institutional Review Board (IRB) submission and approval, specialty subcommittee reviews, as well as FDA, IND, and IDE submissions and maintenance.

• Participates in planning, development, coordination, and implementation of studies that promote and enhance research collaboration with individuals/groups internal and external to the organization.

• Serves as a liaison between principal investigators (PI), co-investigators, sponsoring agents, regulatory bodies, and other members of the research team, leading study teams in meeting internal and external regulatory compliance requirements and serving a vital role during study start-up, monitoring, and audits.

• Partner with PI and study team regarding strategic planning around clinical research portfolios. Establish professional relationships with Contract Research Organizations, Pharmaceutical Sponsors, Funders and Grantors.

• Uses specialized expertise to manage compliance documentation submission and maintenance, compliance training, compliance committee formation, and other programmatic functions.

• Advises the development of a formalized training program for both new and existing staff within the unit and any affiliates and/or partners. Training and onboarding of all research staff in GCP, 21 CFR 11, 21 CFR 312, 21 CF 812 and divisional policies for the conduct of clinical research.

• Prepares, completes, and submits all compliance documentation on a routine basis. Coordinates compliance committee meetings. Plans and executes internal and external audits and activities to support regulatory agency inspections.

• Leads and provides expertise in the implementation of compliance activities designated by the University's strategic plans. Monitors University compliance with regulations and laws.

• Represents the University in regulatory proceedings before federal, state and local agencies. Prepares the University's position statements and responses to information requests. Leads and manages audit responses and negotiations with administrative agencies.

• Performs other related work as needed.

Minimum Qualifications

Education:

Minimum requirements include a college or university degree in related field.
Work Experience:

Minimum requirements include knowledge and skills developed through 7+ years of work experience in a related job discipline.
Certifications:

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Preferred Qualifications

Education:

• Master’s Degree in regulatory affairs, public health, public policy, behavioral science, or a related field.

Experience:

• Experience with cooperative group and industry sponsored FDA regulated clinical trial, and investigator initiated clinical trial site management.

• Interacting with local and central IRBs and other regulatory bodies.

• Developing and maintaining departmental infrastructure for scientific review, feasibility assessment, and protocol effort projection.

• Ensuring compliance of multiple studies with institutional requirements and policies.

• Independently developing, or guiding the development of, complex data entry or collection protocols and tools.

• Setting objectives, goals, and detailed agendas for multidisciplinary meetings.

• Preparing and maintaining FDA regulatory submissions on more than one PI-initiated study overseen by the FDA.

• Handling complex situations and/or potential hold issues directly with the FDA, in collaboration with the PI.

Licenses and Certifications:

• ACRP / SOCRA research certification.

Preferred Competencies

• Familiarity with electronic regulatory submission platforms and Clinical Trial Management Systems.

• Ability to mentors or train others to communicate effectively with CRO and/or sponsor, and in managing and conducting site visits. Understands the relationship between sites, sponsors and CROs in order to solve problems.

• Ability to mentor and train others to ensure that studies are conducted in compliance with institutional requirements and other policies.

• Ability to recognize, in complex scenarios, when all types of agreements (MTAs, CTAs, CDAs, DUAs, DTAs, etc.) are necessary and which procedures to follow, including special terms that may need to be included.

• Demonstrates advanced application and knowledge of monitoring and audits. Trains or leads others in most tasks related to monitoring and audits.

• bility to mentor or train others in meeting preparation and follow up. Facilitate healthy communication during meetings.

• Ability to conduct and document informed consent and assent for multiple interventional and/or complex studies. Exhibit additional knowledge or skills in consent procedures.

• Advanced understanding of sponsor/regulatory reporting.

• Ability to implement systems that ensure quality of data and to train others in data collection and entry.

Application Documents

• Resume (required)

• Cover letter (required)

When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.

Job Family

Legal & Regulatory Affairs
Role Impact

Individual Contributor
Scheduled Weekly Hours

40
Drug Test Required

Yes
Health Screen Required

Yes
Motor Vehicle Record Inquiry Required

No
Pay Rate Type

Salary​
FLSA Status

Exempt​
Pay Range

$110,000.00 - $160,000.00The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.

Benefits Eligible

YesThe University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.

Posting Statement

The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the University's Notice of Nondiscrimination.

Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.

All offers of employment are contingent upon a background check that includes a review of conviction history.  A conviction does not automatically preclude University employment.  Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.

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