Clinical Site Director: Trials Operations & Growth

Velocity Clinical Research, Inc.

Los Angeles (CA)

On-site

USD 140,000 - 160,000

Full time

4 days ago
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Benefits offered by this job

Medical, dental and vision insurance
Paid time off & holidays
401(k) with company match
Annual incentive program

Job summary

Velocity Clinical Research, Inc. is seeking a Clinical Site Director to manage the site’s overall operations, budgets, and clinical trial conduct in accordance with ICH GCPs.

You will oversee staffing, feasibility, recruitment, and regulatory compliance while ensuring patient safety and data integrity. You will lead cross-functional teams, align with sponsors and CROs, and drive operational excellence to accelerate trial timelines across site operations.

Qualifications

  • Bachelor’s degree in a relevant field; advanced degree preferred or equivalent experience.
  • Extensive clinical management experience in clinical research.
  • Strong written and verbal communication, leadership and problem-solving abilities.

Responsibilities

  • Oversee site operations, budget, and study targets.
  • Ensure compliance with ICH GCPs and Velocity SOPs.
  • Lead patient recruitment strategies and site staffing plans.
  • Coordinate with Sponsors, CROs, and IRBs as needed.
  • Develop relationships with external healthcare providers to aid recruitment.

Skills

Project management
Clinical research knowledge
Leadership
Communication skills
English proficiency

Education

Bachelor’s degree in a related field
Advanced degree preferred or equivalent

Tools

MS Office
Clinical Conductor CTMS
CRM systems

Job description

Velocity Clinical Research, Inc. is seeking a Clinical Site Director to manage the site’s overall operations, budgets, and clinical trial conduct in accordance with ICH GCPs.

You will oversee staffing, feasibility, recruitment, and regulatory compliance while ensuring patient safety and data integrity. You will lead cross-functional teams, align with sponsors and CROs, and drive operational excellence to accelerate trial timelines across site operations.

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