Senior / Statistical Programmer (Taiwan)
IQVIA
Taipei, TW
8天前

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.

Statistical Programmer

At IQVIA™ we help healthcare and biopharma companies improve their probability of success. We do this by connecting our scientific, therapeutic and analytics expertise with superior delivery.

From advisory through operations, IQVIA™ and its affiliate companies is now the world’s largest provider of product development and integrated healthcare services.

One of FORTUNE’s Most Admired Companies’, we offer unparalleled scope for a career in world-leading clinical research. Global projects, innovative tools and industry leading customers combine with outstanding support and clear career management which allows you to make a difference and to connect with great opportunities.

Statistical Programmer the role

Whether you are beginning or continuing your career as a programmer, this role is an ideal stepping-stone. You will have training and development to plan and progress your long-

term career in the direction you choose. And you will not have to do it alone you will have dedicated mentoring and development opportunities to help shape your future and improve your skills.

Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects and across therapeutic areas.

You will also be working on programming from scratch with the ability to create new code, discover different opportunities and unusually for a non-

clinical role make a real impact on patient health.

While projects vary, your typical responsibilities and opportunities might include :

  • Programming all aspects of a clinical trial, from files to tables and figures
  • Programming from scratch
  • Working as part of a team
  • Using SAS in a quality control / production capacity
  • Providing leadership to colleagues even from a junior position
  • You will need to be comfortable collaborating and communicating with a variety of colleagues, often teammates located in different parts of the world.

    You will also have the opportunity to attend weekly forums discussing SAS and relevant courses all with the potential to grow your career into more technical or managerial roles.

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