Biostatistician, Late phase research focused - (1807852) in Seoul, KR at IQVIA™

Date Posted: 8/29/2018

Job Snapshot

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.
  • Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures
  • Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results
  • Interpret analyses and write statistical sections of study reports. Provide training, guidance and mentorship to lower level and new staff
  • Communicate with clients regarding study protocol or statistical analysis issues as they arise
  • Develop analysis plans, table shells, programming and table specifications; produce tables, listings and figures; perform data review and statistical analysis.
  • Develop protocol development, sample size calculation, and protocol and case report form (CRF) review.
  • Advise data management staff on database design, validation checks and critical data.
  • Write statistical sections of integrated reports.
  • Provide expert statistical input into and review of statistical deliverables (i.e. analysis plans, table shells, programming and table specifications, data review, tables, listings, figures and statistical sections for integrated reports) and data management deliverables (i.e. database design, validation checks and critical data).
  • Manage project budget and resource requirements. Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage scope, and provide revenue and resource forecasts for single studies.
  • Assist with review of RFPs and QIPs; prepare proposal text and participate in bid defense meetings.
  • Provide training and guidance to lower level and new staff
  • Manage customer relationships.

Job Requirements

Minimum Qualification
  • Bachelor’s degree or educational equivalent in biostatistics
  • 2-5 years relevant work experience in Phase I-IV clinical trials, PMS, or observational study
  • Understanding and knowledge of applicable clinical research regulatory requirements and KFDA/MFDS regulatory requirements
  • Familiarity with statistical methods that apply to applicable clinical trials including PMS
  • Strong working knowledge of SAS computing package
  • Familiarity with other statistical computing packages (e.g. S+, SUDAAN, StatXact, etc)
Additional Qualification
  • Excellent written and oral communication skills including grammatical/technical writing skills
  • Excellent attention and accuracy with details
  • Strong individual initiative
  • Strong organizing skills
  • Strong commitment to quality
  • Ability to effectively manage multiple tasks and projects
  • Ability to solve moderately complex problems
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients
  • Working knowledge of relevant Data Standards
Preferred Qualification
  • Master’s degree or Ph. D. in biostatistics
  • Work experience in CROs or pharma. companies
  • Work experience in late phase study including PMR or observational study
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: 1807852

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