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RWE Clinical Project Manager (FSP)

93 100 - 232 800$
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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Текст:
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TL;DR
RWE Clinical Project Manager (FSP) (Real-World Evidence/Oncology): Leading end-to-end delivery of global observational studies within an oncology-focused pharma environment with an accent on cross-functional coordination, study documentation, vendor management, and financial oversight. Focus on applying primary and secondary data study designs, mitigating operational and quality risks, and delivering complex clinical research programs against scope, timelines, and quality requirements.

Location: Durham, North Carolina, United States of America

Salary: $93,100–$232,800 annualized base pay

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for life sciences and healthcare organizations.

What you will do

  • Lead global, cross-functional teams delivering contracted real-world observational study scope, timelines, and quality.
  • Develop project documentation, including project management plans, study tools, and training materials.
  • Monitor study progress, financial performance, forecasting, and change control.
  • Manage vendors and communications across in-house, hybrid, and outsourced sourcing models.
  • Identify operational and quality risks, implement corrective or preventive actions, and resolve study issues.
  • Generate project and program metrics, report to senior management, and contribute to continuous improvement.

Requirements

  • Bachelor’s degree in life sciences or a related field.
  • 4–6 years of project management or clinical operations experience in pharma, CRO, or an RWE environment.
  • Demonstrated experience leading observational or real-world evidence studies independently.
  • Strong understanding of RWE study designs, clinical research conduct, and applicable clinical research regulatory requirements.
  • Experience with both primary and secondary data collection study designs.
  • Strong organizational, prioritization, communication, decision-making, and stakeholder management skills.

Culture & Benefits

  • Work within the environment of a prominent pharmaceutical company as part of a dedicated RWE FSP team.
  • Collaborate with epidemiologists, data scientists, clinical leads, vendors, program leads, and business stakeholders.
  • Operate in a matrixed, fast-paced, and evolving environment.
  • Health and welfare benefits may be provided in addition to base pay.
  • Incentive plans, bonuses, or other compensation may be available depending on the position.

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