About The Position

Join IQVIA’s Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you’ll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA’s global expertise. Overview: This role provides scientific support for RWE/Epidemiology studies by conducting literature reviews, data cleaning, code look-ups, and quality control activities. The role also contributes to scientific deliverables and supports operational coordination across studies to ensure high-quality execution.

Requirements

  • Strong analytical, organizational, and writing / communication skills
  • Intermediate understanding of epidemiologic methods
  • Ability to independently conduct scientific and operational tasks
  • Ability to identify and escalate operational risks
  • Ability to collaborate effectively with programmers and cross-functional partners

Nice To Haves

  • PhD in Epidemiology preferred, Master's degree required (MPH minimum)
  • Experience in applied epidemiology or scientific operations
  • Experience working in a matrixed, cross-functional team environment
  • Experience supporting development of scientific deliverables

Responsibilities

  • Conducts literature reviews, scientific summaries, data cleaning, code look up, and QC tasks
  • Contributes to development of abstracts, manuscripts, posters, and scientific summaries
  • Support creation of analysis planning documents and table shells, working closely with programmers
  • Provide rapid responses to epidemiology and safety information requests
  • Perform any other relevant scientific tasks as needed to support study progress
  • Provides operational oversight across multiple studies or therapeutic areas
  • Maintain study documentation, trackers, and operational tools to ensure consistent process application
  • Coordinate safety requests, data requests, timelines, and other cross-functional operational needs
  • Supports development and management of study trackers, safety requests, and other operational resources
  • Monitor progress of vendor deliverables and help identify risks or delays

Benefits

  • Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.
  • Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.
  • Access IQVIA’s global network who supports your growth

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Education Level

Ph.D. or professional degree

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