Clinical Research Supervisor

Insight Global; Orlando (FL); On-site; USD 85,000 - 115,000; Full time

Job summary

Insight Global is seeking a Clinical Research Supervisor to support its Digestive Health program, focusing on GI and IBD studies. You will lead a team of Clinical Research Coordinators and collaborate with Principal Investigators, physicians, and research leadership to ensure trials run according to protocol and regulatory standards.

The role emphasizes day-to-day oversight, protocol compliance, adverse event reporting, and overall study operations, with opportunities to drive team performance

Qualifications

• Experience supervising Clinical Research Coordinators.
• Strong knowledge of protocol deviations and regulatory guidelines.
• Experience with AE/SAE reporting and documentation.
• Ability to coordinate with Principal Investigators and study teams.

Responsibilities

• Provide daily leadership and support to a team of Clinical Research Coordinators.
• Serve as primary liaison between Principal Investigators, physicians, coordinators, and research staff.
• Oversee study operations and ensure protocol execution.
• Assign and prioritize study-related responsibilities across the research team.
• Support coordinators with study questions, escalations, and issue resolution.
• Monitor study conduct to ensure compliance with sponsor, regulatory, and institutional requirements.
• Review protocol deviations and ensure appropriate documentation and reporting.
• Identify, document, and support reporting of adverse events and serious adverse events.
• Partner closely with investigators and stakeholders to support study enrollment and execution.
• Assist with process improvements, workflow optimization, and team development.
• Serve as the first point of escalation for research operations issues.

Skills

Leadership experience

Protocol deviations

AE/SAE reporting

PI collaboration

Job description

• Prior leadership, supervisory, or management experience
• Strong understanding of protocol deviations
• Experience with adverse event (AE) and serious adverse event (SAE) reporting
• Experience working directly with Principal Investigators and study teams

Plusses:

• RN
• GI, IBD, Digestive Health, or therapeutic research experience
• CCRC, CCRP, or other research certification

Overview

Our client is seeking a Clinical Research Supervisor to support its growing Digestive Health research program, with a primary focus on GI and IBD studies. This individual will lead a team of Clinical Research Coordinators while partnering closely with Principal Investigators, physicians, and research leadership to ensure the successful execution of clinical trials.

In this role, you will provide day-to-day oversight and support for a team of three direct reports, serving as the first point of escalation for research staff and helping to coordinate study assignments, priorities, and workload across the team. You will play a key role in ensuring studies are conducted in accordance with protocol requirements, regulatory guidelines, and research best practices.

The Clinical Research Supervisor will also serve as a subject matter expert on protocol compliance, protocol deviations, adverse event reporting, and overall study operations. Working closely with investigators and clinical teams, you will help maintain research quality, support staff development, and contribute to the continued growth of our client's Digestive Health research program.

This is an excellent opportunity for an experienced clinical research professional with leadership experience who is looking to take on a highly visible role within a growing research department while remaining actively involved in study operations and clinical trial execution.

Day-to-Day Responsibilities

• Provide daily leadership and support to a team of Clinical Research Coordinators
• Serve as the primary point of contact between Principal Investigators, physicians, coordinators, and research staff
• Oversee study operations and ensure protocols are executed appropriately
• Assign and prioritize study-related responsibilities across the research team
• Support coordinators with study questions, escalations, and issue resolution
• Monitor study conduct to ensure compliance with sponsor, regulatory, and institutional requirements
• Review protocol deviations and ensure appropriate documentation and reporting
• Identify, document, and support reporting of adverse events and serious adverse events
• Partner closely with investigators and stakeholders to support study enrollment and execution
• Assist with process improvements, workflow optimization, and team development
• Serve as the first point of escalation for research operations issues