About City of Hope
City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases.
Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope's translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope™, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hope's specialized cancer expertise.
A National Cancer Institute-designated comprehensive cancer center and a founding member of the National Comprehensive Cancer Network, City of Hope is ranked among the nation's "Best Hospitals" in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.City of Hope's commitment to Diversity, Equity and Inclusion
We believe diversity, equity and inclusion is key in serving our mission to provide compassionate patient care, drive innovative discovery, and advance vital education focused on eliminating cancer and diabetes in all of our communities. Our commitment to Diversity, Equity and Inclusion ensures we bring the full range of skills, perspectives, cultural backgrounds and experiences to our work -- and that our teams align with the people we serve in order to build trust and understanding. We are dedicated to fostering a community that embraces diversity - in ideas, backgrounds and perspectives; this is reflected in our work and represented in our people.Position Summary
The Regulatory Affairs Specialist II is responsible for coordinating and supporting regulatory affairs activities relating to all City of Hope sponsored INDs and investigator-initiated INDs. This includes assistance with preparation of initial Phase I/II clinical trial IND filings and maintenance of the IND in the setting of an academic research organization. The position will assist in the development and implementation of regulatory strategies for interacting with regulatory agencies and will act as a liaison with the FDA, NIH-OBA, and institutional regulatory committees. This position will provide staff expertise and preparatory assistance to Regulatory Affairs management in preparation of documents for Regulatory submissions to applicable regulatory agency(ies). He/she will ensure regulatory affairs compliance of clinical trials under a COH-sponsored IND.Essential Functions:
Basic education, experience and skills required for consideration:
- Under direction of the Director of OIDRA or designee, establishes and implements standards, approaches, methods, and procedures for the various regulatory affairs activities relating to the development and implementation of novel therapeutics.
- Serves as a project lead for portions or all sections of an IND filing, NIH OBA filing, or international filing, as applicable.
- Reviews technical data and reports to ensure consistency of data provided in the IND and other regulatory submissions.
- Prepares for and serves as the regulatory affairs liaison in Trial Initiation Meetings and project meetings for COH-sponsored INDs, as required
- Oversees and organizes documentation of user instructions and the preparesstandard operating procedures (SOPs) for clinical trials conducted under a COH-sponsored IND.
- Provides assistance and support to Principal Investigators, for timely and accurate submissions of annual reports or other regulatory documents required by the FDA. Prepares and files annual reports and other regulatory documents to internal and external regulatory committees as needed.
- Ensures compliance to institutional and federal applicable regulatory and quality policies and FDA guidance rulings, as well as ensuring compliance with Good Clinical Practice (GCP), Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) guidelines for all research programs.
- Assist with preparing, filing and maintaining regulatory documents to COH oversight committees such as OSBC, radiation safety, IBC, CPRMC, IRB, IACUC, and SCRO as needed. Follows HIPAA guidelines.
- Maintains electronic databases of files related to compliance of institutional and federal guidelines and maintain current knowledge of regulations and guidances
- Under direction of the Director or designee, reports all Serious Adverse Events (SAEs) to applicable regulatory agency (ies).
- Assists with preparation of grants and papers with respect to their interaction with regulatory agencies.
- Provides guidance to physicians, CPRMC, PRMC, DSMC and IRB in the interpretation of GCP, IRB, and FDA regulations and guidelines.
- Participate in clinical trials adherence evaluations and compliance audits.
- Participates in the training of staff, as needed.
- Facilitates internal and external regulatory agency inspections.
- Is responsible for continued development and maintenance of quality assurance programs.
- Maintains professional growth and development through seminars, workshops, and professional affiliations to maintain certification/licensure and/or keep abreast of latest trends in the field of expertise.
- Is self-motivated in organizing and following through on assigned projects.
- Ensures work environment is organized and functions efficiently.
- Attends and participates in meetings as required.
- Tolerates flexible work hours to achieve critical deadlines.
Preferred education experience and skills:
- Requires a Bachelors degree in a scientific discipline or equivalent.
- Experience may substitute for minimum education requirements.
- A minimum of 5 to 7 years related experience with a Bachelors or 3 to 6 years with a Masters, or 2 to 5 years with a PhD, and demonstrated working knowledge of scientific principles.
- Up to date familiarity with regulations pertaining to INDs involving CDER, CBER and NIH-OBA activities, including experience as an auditor, quality control coordinator, or compliance officer.
- Computer skills including Microsoft Windows, Word and Excel, Adobe Acrobat.
- Graduate Level Degree in Regulatory Affairs or related field.
- Certification in Regulatory Affairs preferred.
- Must possess excellent written/editorial, interpersonal, verbal communications and computer literacy skills.
- Must communicate technical information in a clear, concise manner.
- Ability to monitor and train other employees.
- Ability to master content across all clinical research areas.
- Previous supervisory experience preferred.
- Preferably has experience with Adobe Framemaker.
- As a condition of employment, City of Hope requires staff to comply with all state and federal vaccination mandates.
City of Hope is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, or status as a qualified individual with disability.