Senior Remote Clinical Trial Manager

Syneos Health, Inc.; North Dakota; Hybrid; USD 110,000 - 160,000; Full time

Job summary

Syneos Health is seeking an experienced professional to lead site management oversight and clinical monitoring across multi-site trials. The role focuses on patient safety, GCP compliance, data integrity, and risk-based monitoring while coordinating with CRAs, CMS, and other functional teams.

You will oversee study tools, dashboards, and CTMS/EDC systems, ensure timely site activations and milestones, and provide training to study teams on protocols and data plans.

Qualifications

• Bachelor’s degree or RN in a related field.
• Demonstrated ability to lead and align teams to achieve milestones.
• Experience working in an international environment.
• Strong site management and monitoring experience.
• Knowledge of Good Clinical Practice (GCP)/ICH guidelines and regulatory requirements.

Responsibilities

• Provide site management oversight and clinical monitoring with focus on patient safety and data integrity.
• Oversee RA/RACT processes, timelines, budgets, and contracted scope.
• Escalate risks to project management and ensure timely delivery of study milestones.
• Coordinate communications with investigators and site staff as needed.
• Collaborate with functional teams to ensure handoffs and milestones are met.
• Develop and maintain study tools, templates, and CTMS/EDC dashboards.
• Coordinate training to study teams on protocol specifics and data collection.
• Oversee resource allocations for CRAs and central monitors and monitor quality of deliverables.
• Review trial management dashboards and systems to ensure timely updates and compliance.
• Provide feedback to line managers and mentor CTMs as required.

Skills

Leadership

Cross-functional collaboration

Problem solving

Communication

Regulatory knowledge

Education

Bachelor’s degree or RN

Tools

CTMS

EDC

Dashboards

Job description

Syneos Health is seeking an experienced professional to lead site management oversight and clinical monitoring across multi-site trials. The role focuses on patient safety, GCP compliance, data integrity, and risk-based monitoring while coordinating with CRAs, CMS, and other functional teams.

You will oversee study tools, dashboards, and CTMS/EDC systems, ensure timely site activations and milestones, and provide training to study teams on protocols and data plans.