Background information about the job or company (e.g., role context, company overview)

IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...

Responsibilities or duties

As a Senior Biostatistician, 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.

You will also collaborate with medical and programming staff to produce interim reports and final reports, allowing a comprehensive understanding and interpretation of the clinical trial data and outcome.

Qualifications or requirements (e.g., education, skills)

BSc or MSc degree in Biostatistics or related field and between 4 - 6 years’ relevant experience

Familiarity with moderately complex statistical methods that apply to applicable clinical trials

Good working knowledge of SAS and CDISC SDTM and ADaM

Ability to effectively manage multiple tasks and project, ability to communicate and explain statistics

Experience needed

4 - 6 years’ relevant experience

Any other provided details (e.g., benefits, work environment, team info, or additional notes)

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• Provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies.
• Act as a statistical team lead for single, complex studies or groups of studies.
• Manage the scope of work and budget, providing revenue and resource forecasts.
• Prepare proposal text and attend bid defense meetings.
• Collaborate with medical and programming staff to produce interim reports and final reports.

• SAS
• CDISC SDTM
• CDISC ADaM
• Ability to effectively manage multiple tasks and projects
• Ability to communicate and explain statistics

• BSc or MSc degree in Biostatistics or related field
• Familiarity with moderately complex statistical methods that apply to applicable clinical trials