Remote Sponsor Clinical Trial Manager

Syneos Health, Inc; Antioquia; Híbrido; COP 279.616.000 - 403.890.000; Jornada completa

Descripción de la vacante

Syneos Health, Inc is seeking a Clinical Trial Manager (Sponsor dedicated) with extensive experience in project management and clinical trial oversight. The role focuses on site management, monitoring, data integrity, and regulatory compliance across studies.

Collaboration with CRAs, central monitors, and other functional teams is essential to drive milestones and risk mitigation. The candidate will engage in risk assessment, planning, and communications with principal investigators and site

Formación

• Bachelor’s degree or RN/related field with relevant clinical trial management experience.
• Strong leadership and ability to drive cross-functional teams across sites and vendors.
• Experience with monitoring strategies, risk-based monitoring, and regulatory compliance.

Responsabilidades

• Oversees site management, site monitoring, and data integrity with focus on patient safety and protocol compliance.
• Manages risk assessment activities and escalates issues affecting timelines, quality, or budget.
• Coordinates planning, training, and resourcing for CRAs and central monitors across studies.
• Ensures CTMS, dashboards and CTMS-related tools are set up and maintained for study teams.
• Provides status updates to stakeholders and coordinates with functional partners to meet study milestones.

Conocimientos

Project management

Clinical monitoring

GCP compliance

Leadership

Educación

Bachelor's degree in life sciences

Herramientas

CTMS

EDC

TMF

ePROs

Descripción del empleo

Syneos Health, Inc is seeking a Clinical Trial Manager (Sponsor dedicated) with extensive experience in project management and clinical trial oversight. The role focuses on site management, monitoring, data integrity, and regulatory compliance across studies.

Collaboration with CRAs, central monitors, and other functional teams is essential to drive milestones and risk mitigation. The candidate will engage in risk assessment, planning, and communications with principal investigators and site