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June

Senior Biostatistician

IQVIA - Melbourne, VIC

Any Industry
Source: uWorkin

JOB DESCRIPTION

Are you a Senior Biostatistician looking for your next challenge?


This position prepares analysis plans and writes detailed specifications for analysis files, tables, listing and figures. The successful candidate will have excellent attention and accuracy with details, strong individual initiative, organizing skills and commitment to quality. They will also have the ability to solve complex problems, provide and accept director of lead team members and establish and maintain effective working relationships with co-workers, managers and clients. This position can be based in any Australia Location

Responsibilities include but not limited too:

  • Develop analysis plans, table shells, and programming and table specifications; produce tables, listings and figures; perform data review and statistical analysis.
  • Assist with protocol development, sample size calculation, protocol and case report form (CRF) review.
  • Advise data management staff on database design, and critical data.
  • May advice on validation checks.
  • Write statistical sections of integrated reports.
  • Under supervision, act as statistical team lead for single studies.
  • Understand the Scope of Work, budget and quote assumptions, estimate the work completed, and manage scope for single studies.
  • May manage project budget and resource requirements and provide revenue and resource forecasts for single studies.
  • Assist with review of RFPs and QIPs; prepare proposal text. May participate in bid defence meetings.
  • Provide training and guidance to lower level and new staff.

Skills and experience required:

  • PhD in biostatistics or related field OR Master's degree in biostatistics or related field and one year relevant experience OR Bachelor's degree or educational equivalent in biostatistics or related field and three years’ relevant experience OR equivalent combination of education, training and experience.
  • In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Familiarity with moderately complex statistical methods that apply to applicable clinical trials.
  • Strong working knowledge of SAS compute package and relevant Data Standards such as CDISC/ADaM.
  • Familiarity with other relevant statistical computing packages such as StatXact.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.