Remote Senior Global Clinical Trial Manager

SoTalent

United States

Remote

USD 120,000 - 180,000

Full time

48 hours ago
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Job summary

SoTalent is seeking a Senior Clinical Trial Manager to lead global Phase I–IV trials from planning to closeout. You will oversee study strategy, cross-functional execution, budgets, timelines, vendors, TMF, and regulatory compliance while providing operational leadership across global teams.

The role requires 7+ years in clinical research and experience in global trial management, with strong stakeholder engagement and project management skills.

Qualifications

  • 7+ years in clinical research, including global trial management
  • At least 3 years in clinical operations leadership
  • Proven experience managing global, multi-center trials
  • Strong knowledge of ICH-GCP and regulatory requirements
  • Experience with study start-up and regulatory planning
  • Experience with TMF/CTMS and other systems
  • Bachelor’s degree in Life Sciences or related field, or equivalent experience

Responsibilities

  • Lead planning, implementation and execution of global Phase I–IV trials.
  • Develop trial strategies, timelines, budgets, recruitment and risk plans.
  • Coordinate cross-functional study teams and lead trial meetings.
  • Oversee external vendors and clinical budgets.
  • Manage TMF activities and essential trial documentation.
  • Review protocols, informed consent forms and clinical study reports.
  • Support feasibility and investigator selection and recruitment strategies.
  • Mentor Clinical Research staff and drive issue resolution.

Skills

Stakeholder management
Communication
Influencing
Project management
Organisational skills

Education

Bachelor’s degree in Life Sciences/Healthcare or related field

Tools

CTMS
TMF
Clinical trial management systems

Job description

SoTalent is seeking a Senior Clinical Trial Manager to lead global Phase I–IV trials from planning to closeout. You will oversee study strategy, cross-functional execution, budgets, timelines, vendors, TMF, and regulatory compliance while providing operational leadership across global teams.

The role requires 7+ years in clinical research and experience in global trial management, with strong stakeholder engagement and project management skills.

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