As a Senior Biostatistician at IQVIA, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas. You will provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies. Acting as a statistical team lead for single, complex studies or groups of studies, you will manage the scope of work and budget, providing revenue and resource forecasts, coupled with preparing proposal text and attending bid defense meetings.
Responsibilities
Act as a statistical team lead for single, complex studies or groups of studies.
Provide statistical consulting and technical support regarding design, statistical analysis, and regulatory submissions.
Manage the scope of work and budget for assigned projects.
Provide revenue and resource forecasts for projects.
Prepare proposal text and attend bid defense meetings.
Collaborate with medical and programming staff to produce interim and final reports.
Facilitate comprehensive understanding and interpretation of clinical trial data and outcomes.
Requirements
BSc or MSc degree in Biostatistics or a related field.
Between 4 - 6 years’ relevant experience in biostatistics.
Familiarity with moderately complex statistical methods that apply to clinical trials.
Good working knowledge of SAS and CDISC standards (SDTM and ADaM).
Ability to effectively manage multiple tasks and projects.
Strong ability to communicate and explain statistics clearly.
How to Apply
Interested and qualified candidates should apply online through the IQVIA careers portal. You can access the application page directly here: IQVIA on jobs.iqvia.com. Follow the instructions on the company website to submit your CV and application details.
How to Apply
Interested and qualified candidates should apply online by visiting the IQVIA application portal: Apply Here.
