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Join us in EMEA Biostatistician II / Senior Biostatistician / Lead Statistician – Based Western Europe - (1624231) in Reading, UK at IQVIA™

Date Posted: 10/11/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Reading, UK
  • Job Type:
  • Experience:
    At least 1 year(s)
  • Date Posted:
    10/11/2018
  • Job ID:
    1624231

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.

We provide actionable solutions by tapping into the power of the IQVIA CORE™:

• Domain Expertise. Institutional knowledge and domain expertise across diseases, geographies and scientific methods

• Advanced Analytics. Faster, more precise decision-making generated by advanced analytics designed for healthcare

• Unparalleled Data. One of the world’s largest curated healthcare data sources with innovative privacy protections

• Transformative Technology. Leading technologies to provide real-time access to operations-critical information

With a global team of 50,000+ working across 100 countries, we harness these insights, commercial and scientific depth, and executional expertise to empower clients to achieve some of their most important goals: Improving clinical, scientific and commercial results.

A career with the Biostatics team at IQVIA™ will connect you to great opportunity to achieve professional success. The size and breadth of our practice is unparalleled in the industry and you will work in a fast-paced environment where innovation is a constant. At IQVIA™ your work will  also impact healthcare around the world as you will be involved with the most important drugs and the highest-profile clients. With clear career paths, a supportive working environment and a flexible working culture, our employees are empowered to drive their careers forwards to match their goals. 


The role


As a Statistical Scientist you will 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 clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates

to timelines, data quality, and interpretation of results.


As part of your responsibilities you will:

  • Coordinate the development of analysis plans, table shells, programming and table specifications, the production of tables, listings and figures, data review and statistical analysis.
  • Perform protocol development, sample size calculation, protocol and CRF review and also advise data management staff on database design, and critical data. May advise on validation checks.
  • Interpret analysis and craft 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).
  • Act as statistical team lead for single complex studies or groups of studies.
  • Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage scope, and provide revenue and resource forecasts for single studies. May manage project budget and resource requirements.
  • Perform the review of RFPs and QIPs, prepare proposal text and attend bid defense meetings.
  • Manage customer relationships and provide training and mentorship to junior staff members and newcomers.

All responsibilities are important job functions unless noted as nonessential (N).



Job Requirements

To meet our needs, you will:

  • Have excellent written and oral presentation skills including grammatical/technical writing skills and pay attention to the details
  • Have 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
  • Take strong individual initiative, show dedication to quality and present excellent organization skills
  • Show deep understanding of SAS computing package
  • Be familiar with other relevant statistical computing packages such as nQuery
  • Lead effectively multiple tasks and projects

You should also be able to:

  • Lead and co-ordinate small teams
  • Solve moderately complex problems
  • Establish and maintain effective working relationships with coworkers, managers and clients
  • Demonstrate deep knowledge of relevant Data Standards (such as CDISC/ADaM)

Qualifications

You should have PhD in biostatistics or related field and 1 year relevant experience; Master's degree in biostatistics or related field and 3 years relevant experience; Bachelor's degree in biostatistics or related field and 5 years relevant experience; or equivalent combination of education, training and experience


Physical requirements

  • Extensive use of telephone, face-to-face communication requiring accurate perception of speech and of keyboard requiring repetitive motion of fingers
  • Regular sitting for extended periods of time
  • Flexibility on travelling

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: 1624231