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