IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients.
Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
Responsibilities Prepare analysis plans and write detailed specifications for analysis files, tables, listings and figures.
Interpret analyses and write statistical sections of study reports. Provide training, guidance and mentorship to lower level and new staff.
Develop analysis plans, table shells, 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 advise 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.
prepare proposal text. May participate in bid defense meetings. Provide training and guidance to lower level and new staff.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill, and / or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Experience Typically requires 2 - 3 years of prior relevant experience. Knowledge Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.
Bachelor's Degree, Biostatistics or related field and 3 years' relevant experience Master's Degree, Biostatistics or related field and 1 year relevant experience Ph.
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 individual initiative Strong organizing skills Strong working knowledge of SAS computing package Familiarity with other relevant statistical computing packages such as StatXact Strong commitment to quality Ability to effectively manage multiple tasks and projects Ability to provide and accept direction of lead team members 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 (such as CDISC / ADaM) Join Us Making a positive impact on human health takes insight, curiosity, and intellectual courage.
It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.
Forge a career with greater purpose, make an impact, and never stop learning. At IQVIA, we have a vision. Where every healthcare decision is based on evidence.
Where data science and human science come together to improve global health. Where new and creative solutions aren't just possible - they are expected.
Thank you for your interest in growing your career with us. It takes insight, curiosity, and intellectual courage to transform healthcare.
The 56,000+ employees of the IQVIA family of companies, including Q2 Solutions, are reimagining a world without the consequences of disease.
We are brave minds bringing powerful ideas to reality. At IQVIA, you can truly make an impact in an environment where you're supported to succeed.
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