Multi-Site Clinical Operations Lead

Alcanza Clinical Research; Sugar Land (TX); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with safe harbor match

Short and long-term disability

Job summary

Alcanza Clinical Research in Sugar Land, TX is seeking a Manager, Clinical Operations to lead the operational performance of the clinical staff across studies and sites. You will ensure execution in line with ICH/GCP and FDA guidelines, coordinating with departments to meet milestones.

The role requires a bachelor’s degree, 2+ years clinical research experience, CRC experience, and management background; bilingual English/Spanish is a plus. On-site position with full-time hours.

Qualifications

• Bachelor’s degree and at least 2 years of clinical research experience.
• At least 2 years as a clinical research coordinator (CRC) required.
• 1+ year of management experience in clinical research preferred; bilingual a plus.

Responsibilities

• Lead the clinical operations team to drive study performance.
• Coordinate delivery with Business Development, Recruitment, Finance, Budgets, Contracts, and Quality.
• Review dashboards and systems to monitor site and patient activities.
• Oversee resourcing allocations, site assignments, and study team output.
• Provide training on protocol specifics, CRF completion, SOPs.
• Ensure adherence to ICH, GCP, FDA guidelines and company policies.

Skills

Project management

Clinical operations

Team leadership

Regulatory compliance

Communication

Problem solving

Time management

Bilingual English/Spanish

Education

Bachelor’s degree in a related field

Tools

Microsoft Office

EHR systems

Web applications

HIPAA compliance tools

Job description

Alcanza Clinical Research in Sugar Land, TX is seeking a Manager, Clinical Operations to lead the operational performance of the clinical staff across studies and sites. You will ensure execution in line with ICH/GCP and FDA guidelines, coordinating with departments to meet milestones.

The role requires a bachelor’s degree, 2+ years clinical research experience, CRC experience, and management background; bilingual English/Spanish is a plus. On-site position with full-time hours.