Research Regulatory Specialist, Institute for Translational Science (Hybrid)

Research Regulatory Specialist, Institute for Translational Science (Hybrid)

Galveston, Texas, United States

New

Research Academic & Clinical

UTMB Health

Requisition # 2606272

EDUCATION & EXPERIENCE

Minimum Qualifications:

Bachelor’s Degree or equivalent and 5 years of related experience

Preferred Qualifications:

• Two (2) years of clinical monitoring experience or Three (3) years’ experience in developing training programs

• Clinical Research Associate (CRA) Certification

• Understands and can apply knowledge of clinical trial designs to trial execution

• Experience in the medical/healthcare industry

Job Description

Provides regulatory expertise to faculty members, principal investigators, and research personnel in ensuring clinical processes are conducted in accordance with good clinical practice (GCP), IRB policies and procedures, sponsor and UTMB policy and guidelines. Responsible for identifying and escalating protocol deviations, noncompliance, and data discrepancies in order to ensure compliance with the study protocols and all applicable regulatory frameworks. Under the direction of the Director of Research Integrity and Regulatory Affairs, the Quality Assurance Specialist performs and manages their portfolio. Assists in the development, implementation and maintenance of regulatory policies and the delivery of timely service to customers.

Scope: This position interacts with organizational units spanning Research Regulations and Compliance (RRC), Research Administration (RA), school and departments, central UTMB administration, University of Texas System, State and Federal agencies, and accrediting organizations

Essential Job Functions

• Provide analytical, technical, and professional support to the Office of Research Integrity and Regulatory Affairs. (RIRA).

• Support all aspects of regulatory compliance including but not limited to Institutional Review Board (IRB) processing and approval, IND/IDE submission and management, and Clinicaltrials.gov listing and reporting

• Serve as a regulatory expert regarding compliance with GCP and the Code of Federal Regulations regarding clinical research and other pertinent regulations

• Provide analysis of study processes to identify opportunities to enhance compliance, efficiency, and effectiveness.

• Troubleshoot clinical trials and activities.

• Manage and maintain databases (quality systems and or trainings).

• May serve as subject matter expertise to Information Technology in support of business objectives and initiatives, especially as it relates to interfacing and supporting the regulatory data.

• Prepare and assist in preparing annual reports and quality trending reports.

• Report the status of the quality levels of staff, systems and production activities.

• Preside over improvement programs.

• Evaluate quality events, incidents, queries, and complaints.

• Development and implementation of standard operating procedures and institutional policies and procedures.

• Monitor regulatory changes and remain current on quality standards, all related legislation and compliance issues

• Compile and prepare materials for submission to regulatory agencies.

• Ensure regulatory rules are communicated through corporate policies and procedures

• May create training and education programs in support of the objectives of RIRA and work with faculty and staff to create relevant education programs.

• Ensure that investigator, vendor, facility and system audits are conducted.

• Communicate any critical compliance risks noted from these activities to senior management.

• Assume a lead role for the preparation, conduct, and responses to regulatory agency.

• Adheres to internal controls and reporting structure.

• Performs related duties as required.

Knowledge/Skills/Abilities

• Assist the individual in successfully performing the role

• Possess understanding of research regulatory requirements including GCP.

• Applied understanding of any applicable regulations (e.g., Good Clinical Practice, FDA CFR, clinical research ethics, HIPAA, and patient privacy laws).

• Competencies and essential skills in the following: cross functional relationships, decision making, execution/ results/ process improvement, customer satisfaction.

• Demonstrated ability to maintain composure in difficult circumstances and to identify and adapt to shifting priorities and competing demands. High attention to detail and accuracy.

• Experience understanding technical, scientific, and medical information.

• Able to foster collaborative and constructive relationships with colleagues, faculty, and management of the university.

• A team player who works effectively in a complex, matrix organization.

• Exceptional organizational skills and a focus on results that ensures timely progress on execution priorities.

Working Environment/Equipment

Standard office environment at UTMB’s main campus or other study locations

Salary Range

Commensurate with experience.

Equal Employment Opportunity

UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.

Compensation