Remote Pharmacovigilance Manager for Global Trials

Worldwide Clinical Trials Holdings, Inc.

EE. UU.

A distancia

USD 90.000 - 178.000

Jornada completa

Hace 2 días
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Descripción de la vacante

Worldwide Clinical Trials is seeking a Manager, Pharmacovigilance to lead PV projects across global trials, ensuring high-quality safety data and regulatory compliance. You will guide teams, manage timelines, and collaborate with sponsors and cross-functional colleagues.

The role emphasizes leadership, mentorship, and advancing patient safety through effective PV oversight, with remote work options for US-based candidates.

Formación

  • Bachelor’s degree in a science-related field, nursing, or equivalent.
  • Minimum 5 years of global pharmacovigilance experience across multiple phases.
  • Demonstrated leadership experience, incl. at least 2 years in people leadership.
  • Strong knowledge of clinical trial safety processes and regulatory reporting.

Responsabilidades

  • Lead pharmacovigilance projects and ensure regulatory compliance.
  • Manage delivery against timelines, quality, and budget.
  • Coach and develop team members for high performance.
  • Resolve study or staff issues with sponsors and cross-functional partners.
  • Maintain expertise in global safety regulations and reporting requirements.
  • Support planning activities including scope, budgets, and bids.
  • Organize training and contribute to recruitment and development efforts.
  • Represent Pharmacovigilance during sponsor audits and initiatives.
  • Provide leadership support as a backup to senior PV leadership.

Conocimientos

Global pharmacovigilance
Leadership
Clinical trial safety
Regulatory knowledge
Stakeholder management
English proficiency

Educación

Science-related bachelor’s degree

Herramientas

Safety databases
Regulatory reporting tools

Descripción del empleo

Worldwide Clinical Trials is seeking a Manager, Pharmacovigilance to lead PV projects across global trials, ensuring high-quality safety data and regulatory compliance. You will guide teams, manage timelines, and collaborate with sponsors and cross-functional colleagues.

The role emphasizes leadership, mentorship, and advancing patient safety through effective PV oversight, with remote work options for US-based candidates.

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