Senior Regulatory Coordinator, Canning Thoracic Institute (CTI), Full-Time, Days

Northwestern Memorial Healthcare•Chicago, IL

2h•$41 - $54

About The Position

The Senior Regulatory Coordinator reflects the mission, vision, and values of NMHC, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. Under the direction of the Stem Cell Transplant and Cell Therapy - Autoimmune Diseases Program Manager, the position will be responsible for all regulatory matters concerning the protection of human subjects for studies conducted in the Program. This position oversees the submission process to the Institutional Review Board (IRB) of new studies being processed through the Program, with a particular focus on highly complex protocols involving more than minimal risk to research subjects. The submission process includes completion of extensive, detailed forms summarizing all aspects of a research study as well as the development of new research subject consent forms. This is made possible by the Senior Regulatory Coordinator’s ability to read and interpret highly specialized research protocols (involving stem cell transplant and cellular therapy products) and through understanding of federal regulations governing medical research. Acting on behalf of Principal Investigators, this position will be responsible for subsequently addressing IRB concerns, questions and requests regarding any aspect of a clinical research study until approval is received. This position will serve as the prime contact liaison between the Principal Investigators, sponsor companies, and the IRB. This position will manage the development of regulatory operating policies and procedures for the Clinical Research core. This position will provide expertise to Investigators on regulatory policies guidelines, compliance reporting, and submissions.

Requirements

Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree; OR appropriate combination of education and experience.
Three year’s of work experience in a regulatory and/or medical research environment having developed a strong working knowledge of clinical research protocols or other relevant experience required.

Nice To Haves

Master’s degree preferred.
Knowledge of or experience in NIH grant writing, applications, administration.
Experience working in oncology and/or familiarity with treatments like stem cell transplant and/or cellular therapies.

Responsibilities

Manages submission of all regulatory documents to the IRB, including development of informed consent forms and protocol review for complex studies involving more than minimal risk to research subjects.
Works independently to complete high-acuity protocol reviews with little need or no need for guidance from investigators and/or Research Team Members.
May prepare submissions to NU Research Ancillary Departments, IND applications and renewals.
Corresponds with the FDA throughout the IND process.
Submits study renewal applications and study progress reports to the IRB.
Trains research staff regarding process of submissions in eIRB.
Provides guidance on form preparation and submission and informs Research staff of critical process and policy issues.
Interprets existing and/or new regulatory requirements, developments and Institutional Regulatory Policies as they relate to human subject’s research in order to effectively communicate regulatory requirements to the research staff.
Maintains current knowledge of federal and institutional guidelines and requirements governing research.
Recommends and implements regulatory process improvements.
Develops and manages the internal monitoring auditing program.
Schedules, prepares and participates in all internal and external program audits (monitoring visits), interacts with regulatory agents, and Sponsor monitors.
Ensures regulatory binders (including e-regulatory Complion binders) are well-maintained, organized and complete.
Communicates with IRB and administrative units, project sponsors and project staff to ensure accuracy of regulatory documents and submissions.
Monitors study closure activities and coordinates project close-out with study sponsors, investigators and the IRB.
Tracks study approvals and expirations to ensure uninterrupted project approval.
Maintains regulatory database and manages electronic filing of all regulatory documents.
Performs other duties assigned.