Serves as primary regulatory contact with study sponsors, regulatory bodies, investigators and study team throughout the study initiation, maintenance and closure process. Responsible for coordinating all aspects of regulatory and administrative oversight requirements for conducting clinical research trials.
This position is currently eligible for a hybrid work schedule with some onsite and some work remote days each week.Job Duties
- Apply a detailed understanding of federal and international regulatory requirements when preparing regulatory review applications.
- Provide regulatory oversight of complex regulatory assignments.
- Assist and advise Investigators on their compliance with federal and international regulatory requirements, obligations and responsibilities that govern the conduct of clinical research studies.
- Conduct regulatory affairs training including but not limited to coordination of multi-center studies where BCM is the coordinating center and RRO SOPs.
- Submit studies to IBC for applicable studies as needed.
- Develop, implement, and maintain appropriate policies, procedures, and standards concerning projects.
- Serve as primary regulatory contact with study sponsors, regulatory bodies, investigators and study team throughout the study initiation, maintenance and closure process.
- Maintain regulatory binders with the above documents as well as IRB approvals and study-related correspondence for each protocol from pre-activation through closeout, making sure to update each document as information changes or the document expires.
- Act as a liaison between institutional review committees, regulatory agencies and the investigators to ensure that protocols obtain applicable approvals, that protocol amendments are submitted appropriately and that annual renewals are obtained.
- Work within the sponsor required SIP and eBinder systems to maintain study compliance.
- Notify IRB and study sponsor of all protocol exceptions, deviations, new information and unanticipated events.
- Participate in feasibility, implementation, and site initiation meetings, teleconferences, monitor visits, research audits and other on-site meetings as required.
- Contribute to the ongoing revision/improvement and implementation of SOPs.
- Assist with regulatory affairs training of entry-level employees as assigned and required reporting to clinical trial databases.
- Assist in other aspects of clinical research as needed.
- Prepare and/or obtain all regulatory documentation for each clinical trial including but not limited to: study-specific FDA Form 1572, investigator signature pages, delegation of authority form, training logs, laboratory certifications and credentials, IRB documentation, IBC submissions/approvals and membership list and the following documents for each investigator: Financial Disclosure Form, Curriculum Vitae, Medical License, institutional Conflict of Interest Form and certifications for Good Clinical Practice, Human Subjects Protection and HIPAA.
- Bachelor's degree.
- Two years of relevant experience.
- Prior experience working in an academic research setting
- Strong attention to detail, time management, and data quality
- Ability to understand and manage the complexities of regulatory documentation
Baylor College of Medicine requires employees to be fully vaccinated -subject to approved exemptions-against vaccine-preventable diseases including, but not limited to, COVID-19 and influenza.
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.