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Epidemiology Research Associate - Real World Evidence - EMEA (R1060510) in Reading, UK at IQVIA™

Date Posted: 5/17/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Reading, UK
  • Experience:
    Not Specified
  • Date Posted:
    5/17/2019
  • Job ID:
    R1060510

Job Description

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

With direct access to the world’s most comprehensive information, analytic and consulting/research resources, and healthcare intelligence tools, Real World Evidence (RWE) experts at IQVIA deliver deep insights into pathway design, effectiveness of healthcare interventions and products, and value for money.

Our global RWE Epidemiology team is a key link in this chain.

We have an exciting opportunity for a Research Associate to join our Global RWE team, to develop their career in a supportive and dynamic environment.

As an Epidemiology  Research Associate, you’ll organize and manage research projects including substantive contribution to study protocols, reports and data collection methods, arranging and attendance at project meetings and traveling to client sites as needed.

You’ll assist in preparation of abstracts, manuscripts and oral presentations along with other related study documents.

Your duties will vary, but could include:

  • Performing critical, systematic literature reviews and providing written summaries as needed.
  • Assisting in preparation of abstracts, manuscripts and oral presentations, including development of slides and posters for presentation of project results at conferences.
  • Drafting significant sections of study protocols, reports, and other client facing documents.
  • Organizing and help manage research projects.
  • Reviewing and providing relevant epidemiological and project-specific comments to statistical analysis plans and analysis output.
  • Reviewing and providing input for scientific tasks including CRF/eCRF development, form previews and other ad hoc project tasks (e.g., regulatory responses, slide deck development).
  • Actively participating in client-facing project meetings and being a recognized member of the project team.
  • Conduct statistical analysis as needed.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™



Job ID: R1060510