Bachelor's degree in healthcare administration, Clinical Research, Public Health, Business Administration, Life Sciences, or a related field required.
Master's degree in healthcare administration, Public Health, Clinical Research, or a related discipline preferred.
Minimum of five years of experience in clinical research administration or related fields.
Minimum of two years in a supervisory or leadership role preferred.
Experience managing clinical research operations, regulatory documentation, and study budgets.
Familiarity with clinical research regulations, IRB processes, and FDA requirements.
Responsibilities
Oversee daily administrative and operational functions of clinical research activities.
Coordinate clinical research projects from start-up to closeout.
Develop and maintain standardized research administration policies and procedures.
Provide support and guidance to principal investigators and research staff.
Monitor study progress, timelines, and operational requirements.
Facilitate communication between research teams, sponsors, and leadership.
Identify opportunities to enhance research processes and efficiency.
Benefits
Comprehensive health insurance options.
Retirement savings plan with company match.
Professional development opportunities.
Flexible work schedule options.
Supportive work environment focused on growth.
Full Job Description
Description
In our time of Company growth, we are seeking a Clinical Research Administrator
Work Location: Bradenton, Florida. As part of this role, you will:
Clinical Research Administration and Operations
Oversee the daily administrative and operational functions of clinical research activities.
Coordinate clinical research projects from initial study start-up through study closeout.
Develop, implement, and maintain standardized research administration policies, procedures, and workflows.
Provide administrative support and guidance to principal investigators, sub-investigators, research coordinators, and clinical research staff.
Monitor study progress, timelines, deliverables, and operational requirements.
Coordinate communication between research teams, sponsors, vendors, and organizational leadership.
Identify opportunities to improve research processes, operational efficiency, and study performance.
Requirements
Bachelor's degree in healthcare administration, Clinical Research, Public Health, Business Administration, Life Sciences, or a related field required.
Master's degree in healthcare administration, Public Health, Clinical Research, or a related discipline preferred.
Minimum of five (5) years of experience in clinical research administration, clinical trial operations, research compliance, or healthcare administration.
Minimum of two (2) years of experience in supervisory management or a leadership capacity preferred.
Demonstrated experience managing clinical research operations, regulatory documentation, study budgets, contracts, and reporting.
Experience working with clinical investigators, research sponsors, CROs, and regulatory agencies.
Experience with clinical research regulations, IRB processes, FDA requirements, and Good Clinical Practice (GCP) guidelines.
