Details:

  • Compensation: $110 - $125k
  • Benefits: Medical, Dental, Vision
  • Employment Classification: Direct Hire
  • Status: On-Site
  • Job ID: 21136
Clinical Trial Manager

Job Title: Clinical Trial Manager

Work Location: Burlington County, New Jersey

Summary:

The Clinical Trial Manager is responsible for overseeing the execution and management of multiple clinical trials across a network of sites, ensuring studies are completed on schedule, within budget, and in compliance with regulatory standards.

Responsibilities:

  • Coordinate and manage the full lifecycle of clinical trials across several sites, ensuring achievement of enrollment and study milestones.
  • Mentor and support site-level staff to maintain high standards of protocol adherence and operational performance.
  • Act as the primary liaison for external partners regarding study updates, quality concerns, and project timelines.
  • Conduct ongoing quality assessments to ensure all trial data and documentation comply with regulatory and GCP standards.
  • Monitor and manage study budgets, including site payments and resource distribution across the network.
  • Facilitate communication between internal teams and external stakeholders to resolve issues and maintain study momentum.
  • Implement corrective actions and process improvements based on quality review findings and feedback.
  • Ensure all trial activities are documented accurately and reported in accordance with regulatory requirements.

Qualifications:

  • Bachelor’s degree in Life Sciences, Healthcare, or a related field.
  • 3 or more years of experience in clinical trial management; experience at clinical sites or site management organizations is valued.
  • Comprehensive understanding of ICH-GCP guidelines and regulatory requirements for clinical research.
  • Demonstrated leadership skills, including the ability to manage and mentor teams across multiple locations.
  • Strong organizational, communication, and problem-solving abilities.
  • Experience with financial oversight, including budgeting and resource allocation for clinical studies.
  • Ability to work collaboratively with diverse stakeholders and adapt to changing project needs.
  • Proficiency in maintaining compliance and quality standards throughout the clinical trial process.

Published Category: Clinical Operations & Development

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