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Statistical Scientist

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Primary Location: Durham, North Carolina, United States Additonal Locations: Boston, MA,USA; Chicago, IL,USA; Dallas, TX,USA; Kansas City, KS,USA; Miami, FL,USA; New York, NY,USA; Portland, Oregon, United States,USA; Seattle , WA,USA Full time R1227085

Job description

Join us on our exciting journey!

From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues. 

We have one of the largest Biostatistics departments within the industry of around 1,100+ staff. Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.

Job Overview:

As a Senior Biostatistician, you will develop statistical methods sections of protocols and review case report forms (CRFs). Acting as a lead on studies, you will prepare analysis plans and write specifications for analysis files, tables, and figures. You will communicate with clients regarding study protocol or statistical analysis issues as they arise and communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. You will interpret analyses and write statistical sections of study reports and will be accountable for controlling costs and maximizing revenue recognition. You will also provide training, guidance and mentorship to lower level and new staff.

Requirements:

  • Bachelor's Degree Biostatistics or related field and 3 - 5 years relevant experience Req Or

  • Master's Degree Biostatistics or related field and 3-5 years relevant experience Req Or

  • Ph.D. Biostatistics or related field and 1 year relevant experience Req

  • Typically requires 3-5 years of prior relevant experience, or equivalent combination of education, training and experience.

  • Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with 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 computing package.

  • Familiarity with other relevant statistical computing packages such as nQuery.

  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

  • Working knowledge of relevant Data Standards (such as Clinical Data Interchange Standards Consortium CDISC/ADaM).

JOIN US

Embrace your curiosity and grow your career in an exciting environment where development is a priority.

Think boldly and disrupt conventional thinking.

Enjoy what you do.

Whatever your career goals, we are here to ensure you get there!

Join us on our exciting journey!

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.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.

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