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11 дней назад

Senior Safety Project Lead (Pharmacovigilance)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
China
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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TL;DR
Senior Safety Project Lead (Pharmacovigilance): Managing customer-facing delivery of clinical trial and post-market Lifecycle Safety projects with an accent on project governance, solution design, financial management, and regulatory compliance. Focus on developing tailored safety proposals, leading bid defenses, coordinating cross-functional delivery, and resolving complex customer and operational requirements.

Location: Shanghai, China

Company

Global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Manage customer interfaces, communications, deliverables, timelines, scope, quality, and project financials for assigned Lifecycle Safety projects.
  • Lead clinical trial and post-market safety service delivery across internal teams, customers, and oversight groups.
  • Act as a Safety Subject Matter Expert and solution architect for proposals, budgets, customized solutions, presentations, and bid defenses.
  • Support project start-up, risk identification, mitigation planning, service transitions, and ongoing delivery in line with standard operating procedures.
  • Partner with Sales and Proposals to develop tailored opportunities and strengthen customer relationships.
  • Support audits and inspections, corrective action plans, financial analysis, invoicing, revenue recognition, and change orders.

Requirements

  • Bachelor’s degree in health science or a directly related field, or an equivalent combination of education, training, and experience.
  • 2–3 years of Lifecycle Safety experience, including pharmacovigilance, CEVA, medical information, safety publishing, or risk management, with project management experience.
  • Knowledge of global, regional, and local clinical research regulations, including Good Clinical Practice, ICH guidelines, and standard operating procedures.
  • Strong planning, prioritization, organization, communication, presentation, reporting, delegation, negotiation, and problem-solving skills.
  • Ability to manage multiple projects and competing priorities, work independently, handle ambiguity, and establish effective relationships with customers and colleagues.
  • Knowledge of business operations, financial analysis, tactical planning, and budgeting.

Culture & Benefits

  • Cross-functional collaboration with global management, integrated partners, Sales, Proposals, Quality Assurance, and Lifecycle Safety teams.
  • Opportunities to develop specialist expertise and contribute to departmental or global initiatives.
  • Exposure to customer-facing strategy, solution development, commercial activities, and operational delivery.

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