Global Clinical Trials Project Manager

Worldwide Clinical Trials

Miami (FL)

Presencial

USD 112 000 - 222 000

Tempo integral

14 dias+

Uma candidatura completa num minuto

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Resumo da oferta

Worldwide Clinical Trials in Miami, FL, is seeking an experienced Project Manager to oversee Phase I–IV clinical trials across local, regional, and global scopes. You will lead core project teams, coordinate with functional leads, and ensure on-time, on-budget delivery while meeting quality standards.

The role requires five years of clinical pharma project management, knowledge of ICH/GCP, travel readiness, and strong communication.

Qualificações

  • Minimum five years of clinical pharmaceutical industry project management experience.
  • Knowledge of ICH Guidelines and GCP; familiarity with international regulatory requirements.
  • Willingness to travel domestically and internationally; valid passport.

Responsabilidades

  • Lead core project team members and facilitate their ability to lead extended/complete project team.
  • Coordinate cross-unit coordination with internal and external stakeholders, including sub-contractors.
  • Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources.
  • Ensure design, implementation, tracking and revision of project plans for assigned projects.
  • Promote effective teamwork among project team members; resolve conflicts as needed.
  • Ensure appropriate communication on project-related matters with the PM Management.

Conhecimentos

Project management
Cross-office coordination
Resource planning
Communication skills
Organizational skills
Problem solving

Formação académica

Life science degree

Descrição da oferta de emprego

Worldwide Clinical Trials in Miami, FL, is seeking an experienced Project Manager to oversee Phase I–IV clinical trials across local, regional, and global scopes. You will lead core project teams, coordinate with functional leads, and ensure on-time, on-budget delivery while meeting quality standards.

The role requires five years of clinical pharma project management, knowledge of ICH/GCP, travel readiness, and strong communication.

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