Sr Clin Research Reg Supt Spec

This position represents the Research Base to all regulatory bodies. The Regulatory Specialist is also responsible for ensuring that the work of over 1000 clinical research professionals, as it pertains to regulatory compliance, is complete, accurate, and done in a timely manner as defined by our research protocols, SOPs, and federal requirements. The URCC NCORP Research Base is a large, complex, and dynamic operation involving many investigators, cross-functional teams, and laboratories. This program is funded by a $36 million NIH grant and provides the infrastructure to conduct large multi-site cancer control and cancer care delivery clinical trials within our national network. The Research Base’s network is comprised of over 800 community oncology practices and thousands of oncologists, advanced practice providers, pharmacists, administrators, research nurses, clinical research coordinators, data managers, regulatory specialists, and quality assurance staff nationwide. The Research Base portfolio includes prospective, cohort, and longitudinal Phase II – III randomized clinical trials. This position oversees all regulatory submissions and regulatory compliance and requires a high attention to detail.

Responsibilities

This position represents the Research Base to all regulatory bodies; Acts as primary regulatory liaison with agencies such as IRB, government agencies and Sponsors; Works closely with Research Base cross-functional teams in preparation of study documents for submissions of new protocols, study protocol amendments, annual continuing reviews of approved studies, as well as unanticipated events to the Sponsor and IRB; Performs final edits and proofreading of protocol submission package documents; Prepares and sends protocol documents for submission; Coordinates, tracks and monitors information regarding protocol submissions and documents required for the NCORP sites; Reviews regulatory and other site records such as Federal Wide assurance and site level approvals to ensure our clinical research sites and personnel are adhering to Research Base SOPs, the approved clinical research protocol, and to all applicable federal regulations; Develops and maintains standard operating procedures in collaboration with Program Managers, Administrative leadership, and MPIs of the Research Base; Updates and maintains ClinicaTrials.gov records; Updates and maintains conflict of interest records; Develops, updates and maintains protocol templates; Acts as regulatory representative for NCORP Research Base as primary point of contact for over 800 community sites across approximately 30 NCORP community partner programs; Participates in meetings with regulatory/audit team, project teams and Institutional Review Board meetings as the; Disseminates updates from pertinent meetings to multiple teams within the Research Base and the Division; Oversees, organizes, tracks rostering and membership requests; Perform other project coordination activities as directed by the Program Manager, Administrative leadership, or MPIs of the URCC NCORP Research Base; Assists or leads sections for URCC NCORP progress report reporting and grant submissions for concepts and the overall URCC NCORP Research Base; Other duties as assigned

Requirements

Bachelor's degree and 3 years of relevant experience required; Or equivalent combination of education and experience; Fully adheres to applicable safety and/or infection control standards required; CCRP - Certified Clinical Research Professional by the Association of Clinical Research Professionals (ACRP) within 1 year required; or SOCRA - Certification In Clinical Research within 1 year required; or CHRC - Certified in Healthcare Research Compliance within 1 year required

Nice to have

Ability to mentor and provide training to junior members of the team; Ability to effectively manage moderately complex research protocols/procedures; Possesses a high degree of self-motivation; Recognized ability to function independently; Proficient in managing multiple and competing priorities/demands; Detailed-oriented in record keeping and research documentation; Understands and follows data integrity standards and processes; Thorough knowledge of and established track record in assuring GCP, Responsible Conduct of Research standards, applicable safety standards, OSHA guidelines, throughout study implementation; Strong interpersonal, communication, and organizational skills; Ability to build collaboration among research team members, laboratory staff, patients and families, clinical services; Proficient in MS Office (e.g. Word, Excel, and PowerPoint), email, internet