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9 дней назад

Associate Director, Group Lead, Data Management Reporting and Analytics

124 400 - 207 400$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Релокация
US
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
Associate Director, Group Lead, Data Management Reporting and Analytics (Clinical Data): Leading high-complexity data management, reporting, and analytics initiatives for pharmaceutical and clinical-trial operations with an accent on regulatory requirements, data standards, relational databases, and data visualization. Focus on developing data solutions, managing cross-functional teams and resources, and solving complex problems while guiding strategic decisions across global business units.

Location: Hybrid in the United States, with the primary location in Groton, Connecticut; global-hours collaboration required. The role is posted for additional U.S. locations, including Pearl River, New York City, Collegeville, Tampa, and Cambridge. Permanent U.S. work authorization is required.

Annual base salary: $124,400–$207,400. Tampa, Florida salary range: $111,900–$186,500. The role is also eligible for a 17.5% performance bonus and a share-based long-term incentive program.

Company

hirify.global develops medicines and healthcare solutions supported by evidence-based medical and clinical data.

What you will do

  • Set objectives and lead high-complexity data management, reporting, and analytics projects within a global business unit.
  • Allocate people, technology, and financial resources, including resources outside direct reporting lines.
  • Develop solutions for complex business and clinical data problems and support innovation initiatives.
  • Lead teams, assess talent needs, coach managers, and build a diverse talent pipeline.
  • Partner with global business unit leadership to implement strategy and oversee operational activities.
  • Influence senior management decisions through cross-functional collaboration and knowledge sharing.

Requirements

  • BA/BS with at least 6 years of experience, MBA/MS with at least 5 years, PhD/JD with at least 1 year, or MD/DVM with any level of experience.
  • Relevant experience in pharmaceutical, biotech, CRO, or regulatory agency environments.
  • Experience managing complex projects and developing partnerships across functional areas.
  • Deep understanding of regulatory requirements and relevant data standards.
  • Strong communication, decision-making, influencing, negotiation, project management, and people management skills.
  • Technical proficiency with relational databases and data visualization tools.

Nice to have

  • Knowledge and experience with CDISC.
  • Experience creating data management plans, preparing and validating data, and supporting clinical-trial data reporting.
  • Experience creating data capture solutions and improving existing processes and products.
  • Experience using generative AI tools such as ChatGPT or Microsoft Copilot, including responsible AI and risk management practices.

Culture & Benefits

  • Hybrid work location with collaboration across global time zones.
  • 401(k) plan with company matching and an additional retirement savings contribution.
  • Paid vacation, holidays, personal days, caregiver and parental leave, and medical leave.
  • Medical, prescription drug, dental, and vision coverage.
  • Relocation assistance may be available based on business needs and eligibility.

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