Clinical Research Coordinator-Supervisor

Kelly Science, Engineering, Technology & Telecom; United States; On-site; USD 85,000 - 110,000; Full time

Job summary

Kelly® Science & Clinical in Dallas, TX seeks a Clinical Research Supervisor to oversee day-to-day clinical operations, supervise coordinators, and manage multiple studies. The role balances leadership with hands-on oversight in a fast-paced biotech setting.

The successful candidate will guide study execution, ensure timelines are met, and engage sponsors to maintain strong relationships while driving process improvements across the site.

Qualifications

• 3–4 years of clinical research experience with prior team leadership.
• Strong understanding of clinical study timelines and execution.
• Experience in ALS or cosmetic clinical research is highly desirable.
• Familiarity with Cutometer, Tewameter, Corneometer, VISIA and Chromameter is a strong plus.
• Excellent coaching, communication, and client-facing skills.

Responsibilities

• Lead, coach, and develop a team of Clinical Research Coordinators and staff.
• Oversee study timelines, documentation, trackers, and post-study activities.
• Maintain daily presence in the clinic for operational support.
• Manage a small portfolio of studies and supervise site operations.
• Ensure optimal workload management and resource utilization.
• Foster accountability, engagement, and continuous improvement.
• Address performance concerns and support professional development.
• Serve as client-facing representative to sponsors and maintain relationships.
• Identify and implement process improvements to enhance study execution.

Skills

Leadership

Project management

Coaching & communication

Client-facing skills

Tools

Cutometer

Tewameter

Corneometer

VISIA

Chromameter

Job description

Kelly® Science & Clinical is seeking a Clinical Research Supervisor for a direct-hire position at an early-stage, innovation-driven biotech client in the Dallas Metro area, TX. If you’re passionate about advancing clinical research and ready to take a leadership role in a dynamic environment,

Position Overview:

The Clinical Research Supervisor is a highly visible, hands‑on leadership role responsible for the successful day-to-day execution of clinical research operations at the Dallas site. As the central point of coordination for study activities and team performance, you'll foster a culture of accountability, collaboration, and continuous improvement. You'll supervise Clinical Research Coordinators, oversee a portfolio of active studies, and remain actively engaged in clinic operations. This role balances operational oversight with direct management of 5-6 studies, requiring strong presence, real-time support, and proactive problem‑solving.

Key Responsibilities:

• Lead, coach, and develop a team of Clinical Research Coordinators and research staff.
• Oversee study timelines, documentation, trackers, and post-study activities for compliance and timely deliverables.
• Maintain daily presence in the clinic, offering operational support and guidance.
• Manage a small portfolio of studies while overseeing broader site operations.
• Ensure optimal workload management and resource utilization.
• Foster a culture of accountability, engagement, and continuous improvement.
• Address performance concerns and support professional development.
• Serve as a client-facing representative to sponsors and maintain sponsor relationships.
• Identify and implement process improvements to enhance study execution

Preferred Qualifications:

• 3-4 years of clinical research experience and prior team leadership experience.
• Strong understanding of clinical study timelines and execution.
• Experience in ALS or cosmetic clinical research highly desirable.
• Familiarity with devices such as the Cutometer, Tewameter, Corneometer, VISIA, and Chromameter is a strong plus.
• Excellent coaching, communication, and client-facing skills.

Success Measures (First 3-6 Months):

• Rapid proficiency in client's processes and systems.
• Improved team accountability and operational efficiency.
• Consistently met study timelines and deliverables.
• Optimized workload and balanced clinic/administrative duties.
• Strengthened employee engagement and team collaboration.

This is an excellent opportunity for a clinical research professional who enjoys leading people, solving operational challenges, creating structure, and helping teams thrive in a fast-paced, high-impact clinical setting.