Clinical Operations Manager
Lewisville, TXFull-time
40–42 an hour
Behavioral Health Market Context
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Benefits
Paid Time OffDental CoverageHealth Insurance
Job Description
Good Clinical Practice (GCP).
The Clinical Operations Manager plays a critical leadership role by translating clinical study protocols into operational plans, ensuring clinical research teams operate effectively, and maintaining inspection-ready clinical trial documentation. This position focuses on operational oversight and team leadership rather than routine patient visit coordination or data entry.
This is an excellent opportunity for an experienced clinical research professional who enjoys building high-performing research teams and delivering high-quality clinical trial operations.
What you will do
Clinical Trial Operations Leadership
• Lead the operational execution of clinical trials from study start-up through closeout
• Translate study protocols into site-level operational plans including staffing, recruitment strategies, and visit workflows
• Monitor study timelines, enrollment performance, and operational milestones
• Ensure research activities are conducted in compliance with study protocols, FDA regulations, and ICH-GCP guidelines
Operational Performance and Oversight
· Monitor key operational indicators including enrollment performance, monitoring visit follow-ups, data query timelines, and protocol deviation trends
Pay: $40.00 - $42.00 per hour
Benefits:
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Work Location: In person
The Clinical Operations Manager plays a critical leadership role by translating clinical study protocols into operational plans, ensuring clinical research teams operate effectively, and maintaining inspection-ready clinical trial documentation. This position focuses on operational oversight and team leadership rather than routine patient visit coordination or data entry.
This is an excellent opportunity for an experienced clinical research professional who enjoys building high-performing research teams and delivering high-quality clinical trial operations.
What you will do
Clinical Trial Operations Leadership
• Lead the operational execution of clinical trials from study start-up through closeout
• Translate study protocols into site-level operational plans including staffing, recruitment strategies, and visit workflows
• Monitor study timelines, enrollment performance, and operational milestones
• Ensure research activities are conducted in compliance with study protocols, FDA regulations, and ICH-GCP guidelines
Operational Performance and Oversight
· Monitor key operational indicators including enrollment performance, monitoring visit follow-ups, data query timelines, and protocol deviation trends
Pay: $40.00 - $42.00 per hour
Benefits:
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance
Work Location: In person
Qualifications
Benefits
- •Pay: $40.00 - $42.00 per hour
- •Dental insurance
- •Health insurance
- •Paid time off
- •Vision insurance
Responsibilities
- •This role oversees study planning, research staff performance, patient recruitment operations, regulatory compliance, and study execution to ensure clinical trials are conducted efficiently and in accordance with sponsor requirements and Good Clinical Practice (GCP)
- •The Clinical Operations Manager plays a critical leadership role by translating clinical study protocols into operational plans, ensuring clinical research teams operate effectively, and maintaining inspection-ready clinical trial documentation
- •This position focuses on operational oversight and team leadership rather than routine patient visit coordination or data entry
- •This is an excellent opportunity for an experienced clinical research professional who enjoys building high-performing research teams and delivering high-quality clinical trial operations
- •Lead the operational execution of clinical trials from study start-up through closeout
- •Translate study protocols into site-level operational plans including staffing, recruitment strategies, and visit workflows
- •Monitor study timelines, enrollment performance, and operational milestones
- •Ensure research activities are conducted in compliance with study protocols, FDA regulations, and ICH-GCP guidelines
- •Operational Performance and Oversight
- •Monitor key operational indicators including enrollment performance, monitoring visit follow-ups, data query timelines, and protocol deviation trends
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