Clinical Trials Assistant Director - Regulatory
University of Oklahoma · Oklahoma City, OK · 1 mo ago
AnalystFull-time
About the role
The Clinical Trials Assistant Director- Regulatory provides senior-level administrative leadership for the Stephenson Cancer Center Clinical Trials Office (SCC CTO) regulatory team, overseeing the daily execution of regulatory operations and processes. This role is responsible for managing workflows, monitoring timelines, and tracking the progress of all clinical trials administered by the SCC CTO to ensure alignment with National Cancer Institute (NCI) requirements, institutional priorities, and strategic initiatives.
Responsibilities
- Oversee the daily execution of regulatory operations and processes for the SCC CTO.
- Manage workflows, monitor timelines, and track the progress of all clinical trials.
- Ensure compliance with NCI requirements, institutional priorities, and strategic initiatives.
- Place a strong emphasis on people leadership, including staff recruitment, retention, development, and performance management.
- Foster a culture of quality, accountability, and professional growth.
- Collaborate effectively with internal and external stakeholders.
- Promote operational excellence and keep the team informed of industry best practices and evolving regulatory standards.
Requirements
- Bachelor's Degree in related field.
- 60 months management/supervisory experience in a related field.
- If a Nurse or Physician Assistant, Nurse Practitioner, requires a license through the State of Oklahoma.
Qualifications
- Will accept 48 months related experience in lieu of the Bachelor's Degree for a total of 108 months related experience.
Skills
- Strong leadership skills.
- Excellent organizational and project management abilities.
- Ability to work effectively in a multidisciplinary environment.
- Knowledge of regulatory standards and best practices.
Benefits
- Eligible.
Pay
Pay Range: Commensurate with education and experience.
Schedule
Work Schedule: Monday – Friday, Standard/Fixed Schedule.