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7 часов назад

Safety Project Manager (Pharmacovigilance)

86 000 - 214 800$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

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TL;DR
Safety Project Manager (Pharmacovigilance): Managing regional and global Lifecycle Safety projects for clinical-trial and post-market services with an accent on customer delivery, project finances, regulatory compliance, and cross-functional leadership. Focus on designing Safety solutions for new opportunities, guiding proposals and bid defenses, controlling project performance, and maintaining quality across delivery and audit activities.

Location: Durham, North Carolina, United States of America

Salary: $86,000–$214,800 annualized base pay

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Manage customer interfaces, communication, deliverables, timelines, scope, quality, and financial performance for regional and global Lifecycle Safety projects.
  • Lead customer-facing activities from scoping and proposal development through bid defense, project transition, service delivery, renewal, and extended business opportunities.
  • Act as a Safety subject matter expert and solution architect, developing operational strategies, budgets, customized proposals, presentations, and pricing defenses.
  • Coordinate virtual Lifecycle Safety project teams, internal and external stakeholders, operational teams, sales, proposals, quality assurance, and senior leadership.
  • Oversee project finances, including revenue recognition, invoicing, budget reviews, financial analysis, change orders, direct costs, timesheet costs, and contribution margin.
  • Identify project risks, support audits and inspections, develop corrective action plans, and implement mitigation measures for reliable delivery.

Requirements

  • Bachelor’s degree in health science, a directly related field, or equivalent experience.
  • Four to six years of clinical research experience in a contract research organization or pharmaceutical company, including four years in Lifecycle Safety and two years in project management.
  • Strong knowledge of global, regional, and local clinical research regulations, including Good Clinical Practice and International Conference on Harmonization guidelines.
  • Working knowledge of Lifecycle Safety service lines such as pharmacovigilance, CEVA, Medical Information, Safety Publishing, and Risk Management.
  • Strong project planning, organization, leadership, communication, negotiation, delegation, conflict management, presentation, and problem-solving skills.
  • Business acumen and financial analytical skills, including tactical planning and budgeting, with the ability to manage multiple projects and competing priorities.

Culture & Benefits

  • Cross-functional collaboration across regional and global Lifecycle Safety teams and integrated partners.
  • Customer-centric work focused on service delivery excellence, relationship building, loyalty, and contract renewal.
  • Opportunities to develop specialist expertise and contribute to departmental, regional, and global initiatives.
  • Health and welfare benefits may be provided, along with incentive plans, bonuses, or other compensation depending on the position.

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