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9 дней назад

Senior Patient Safety Vendor Management Manager

120 000 - 171 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US/Denmark
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Patient Safety Vendor Management Manager (Pharmacovigilance): Managing contracts, suppliers, and safety information reporting for patient support programs, market research, call centers, digital health initiatives, social media monitoring, and registries with an accent on PVA compliance, quality monitoring, and regulatory readiness. Focus on reconciling supplier safety data, performing root cause analysis and corrective actions, maintaining pharmacovigilance systems and SOPs, and coordinating with internal teams, business partners, and FDA personnel.

Location: Plainsboro, New Jersey, United States; 0–10% overnight travel required.

Base compensation: $120,000–$171,000 annually, plus potential bonus and long-term incentive compensation.

Company

Global healthcare and pharmaceutical company developing medicines and solutions for diabetes, obesity, rare diseases, and other serious chronic conditions.

What you will do

  • Manage contracts, suppliers, and vendor-related activities supporting Patient Safety and safety information reporting.
  • Oversee Patient Support Programs, Market Research Programs, call centers, digital health initiatives, social and digital media monitoring services, and registries.
  • Monitor safety information reconciliation and quality control activities to ensure compliance with Pharmacovigilance Agreements.
  • Maintain pharmacovigilance oversight data, support the Pharmacovigilance System Master File, and manage the Patient Safety Contracts Management mailbox.
  • Identify and document late supplier reports, perform root cause analysis, and coordinate corrective and preventive actions.
  • Support audits, inspections, training, business continuity, process improvement, and major initiatives.

Requirements

  • Bachelor’s degree in a medical or life science field and at least 8 years of relevant experience, or healthcare professional qualification with at least 5 years of experience including 3 years in safety reporting.
  • Knowledge of FDA requirements, safety information reporting, GMP regulations, and ICH guidance.
  • Experience with contract or alliance management in the pharmaceutical industry is preferred.
  • Strong organizational, project management, communication, and prioritization skills.
  • Intermediate proficiency in Windows, Microsoft Word, PowerPoint, and Excel.

Culture & Benefits

  • Collaborative, patient-centered environment within the Clinical, Medical and Regulatory organization.
  • Medical, dental, and vision coverage, life and disability insurance, and a 401(k) savings plan.
  • Flexible spending accounts, employee assistance, tuition reimbursement, and voluntary insurance benefits.
  • Sick time, flexible vacation, and parental leave policies.
  • Inclusive recruitment process and equal employment opportunity.

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