
Project Manager – Clinical Trial Operations
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in United States.
• Oversee primary project management for clinical research studies within the ACTG Clinical Trials Network.
• Manage technical projects or segments of larger technical programs per contract requirements and company policies.
• Direct and supervise resources assigned to project tasks and activities.
• Guide technical direction throughout project design, implementation, and testing phases.
• Act as the sole point of contact for project development and execution.
• Lead projects from initial concept through to final implementation.
• Collaborate with end users, computer services, client services, and all departments impacted by projects.
• Define the scope and objectives of each project.
• Create work plans, schedules, project estimates, resource plans, and status updates.
• Conduct project meetings and monitor and evaluate project progress.
• Ensure adherence to quality standards and review project deliverables.
• Integrate vendor tasks and monitor and assess vendor deliverables.
• Offer technical and analytical support to the project team.
• Lead problem analysis and solutions for project-related issues.
• Supervise comprehensive clinical trial operations, including study initiation, site coordination, protocol execution, enrollment monitoring, and study closure.
• Hold responsibility for resolving issues.
• Bachelor’s degree in public health, life sciences, health administration, or a related field with 4+ years of clinical trial operations experience, or a Master’s degree with 2+ years of clinical trial operations experience (preferred).
• Strong understanding of regulatory requirements, including GCP, ICH, and FDA/NIH guidelines.
• Demonstrated ability to collaboratively manage complex projects.
• Exceptional communication, organizational, and problem-solving abilities.
• PMP certification is preferred.
• Experience in supporting clinical trials in infectious diseases or related therapeutic areas is preferred.
• Prior involvement with large, multi-site clinical research programs or networks is preferred.
• Personal Time Off (PTO)
• Medical insurance
• Dental insurance
• Vision insurance
• Supplemental life insurance with AD&D
• Short-term disability
• Long-term disability
• Flexible spending accounts
• Parental leave
• Legal services
• 401(k) Retirement Plan with a matching component
• Training and career development opportunities
• Access to a best-in-class e-learning suite for formal and informal education
• Preparation for professional and technical certification
• Education assistance at accredited institutions
• Performance incentives and program-specific awards
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