Senior Director - Clinical Research _ Office of Associate Vice Chancellor for Research

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Human Resources

Important Applications Instructions:

Please complete this application in entirety by providing all of your work experience, education and certifications/

license.  You will be unable to edit/add/change your application once it is submitted.

Job Requisition ID:

R00050168

Job Category:

Research

Organization:

OAVCR-Research

Location/s:

Main Campus Jackson

Job Title:

Senior Director - Clinical Research _ Office of Associate Vice Chancellor for Research

Job Summary:

Leads and oversees the clinical trials operations at the University of Mississippi Medical Center (UMMC). This role is responsible for providing strategic direction, operational leadership, and centralized oversight of clinical research activities. Serves as a key resource for faculty, staff, and institutional leadership, promoting and supporting clinical research efforts while ensuring alignment with regulatory requirements and institutional priorities. Works collaboratively across departments to enhance efficiency, strengthen research capabilities, and facilitate high-quality clinical trial execution.

Education & Experience

Education and Experience Required:

Bachelor's degree and seven (7) years of work experience in clinical research operations, regulatory compliance, or clinical trials management, including two (2) years of experience in a supervisory role.

Certifications, Licenses, or Registration required:

N/A

Preferred Qualifications:

Master’s degree. Society of Clinical Research Associates (SoCRA) Certified Clinical Research Professional (CCRP). Professional level clinical research experience in an academic medical center.

Knowledge, Skills & Abilities

Knowledge, Skills, and Abilities:

Detail-oriented with knowledge in multiple areas of clinical research, including clinical procedures, compliance, government regulations, and budgetary issues. Demonstrates leadership, including proven ability to function effectively in a matrix organization. Experience with information technology and systems analysis. Strong organization, planning, and prioritization skills. Effective decision-making, analysis, and problem-solving abilities supported by critical thinking. Excellent oral and written communication skills, including public speaking.

Responsibilities

• Evaluates current clinical trials practices, sets a vision based on findings, and communicates vision to relevant stakeholders
• Works with Office of the Associate Vice Chancellor (OAVCR) Directors to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes.
• Plans and implements program operations, identifies and develops centralized governance, processes and/or guidelines, coordinates program activities and timelines.
• Assesses communication and training needs, develops and implements any applicable communication, education, training, on-boarding and/or mentorship needs.
• Provides Clinical Trials updates, including trial status/metrics, budget, accomplishments and risks to research leadership and other relevant stakeholders.
• Collaborates with internal and external key collaborators including departments, leaders across the organization, representatives from external