Hybrid Clinical Trial Manager Mexico City

Syneos Health, Inc.

Ciudad de México

Hybrid

MXN 900,000 - 1,300,000

Full time

4 days ago
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Job summary

Syneos Health in Mexico City is seeking a Clinical Trial Manager (CTM) to oversee site management, monitoring, and central monitoring deliverables with emphasis on patient safety and data integrity. You will coordinate CTMS, EDC, eDiary and other systems; lead CRAs and central monitors; manage risks, timelines, and budgets, while collaborating across Study Start Up, Data Management and Recruitment teams.

Applicants should hold a Bachelor's or RN, have GCP/ICH knowledge, and strong communication

Qualifications

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
  • Ability to lead and align teams in the achievement of project milestones.
  • Capable of working in an international environment.
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
  • Moderate travel, approximately 20%.
  • Good computer skills; strong communication, presentation and interpersonal skills.

Responsibilities

  • Oversee site management, clinical monitoring and central monitoring deliverables.
  • Manage risks to timelines, quality and budget; escalate as needed.
  • Coordinate CTMS, EDC, eDiary, TMF and other systems for site activities.
  • Train study team on protocol specifics, data plans and timelines.
  • Ensure regulatory compliance and patient safety throughout the study.
  • Support site activation, enrollment targets and milestones.

Skills

Team leadership
Budget management
Risk-based monitoring
GCP/ICH knowledge
Communication skills
Problem solving

Education

Bachelor’s degree or RN in a related field

Job description

Syneos Health in Mexico City is seeking a Clinical Trial Manager (CTM) to oversee site management, monitoring, and central monitoring deliverables with emphasis on patient safety and data integrity. You will coordinate CTMS, EDC, eDiary and other systems; lead CRAs and central monitors; manage risks, timelines, and budgets, while collaborating across Study Start Up, Data Management and Recruitment teams.

Applicants should hold a Bachelor's or RN, have GCP/ICH knowledge, and strong communication

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