[Hiring] Senior Biostatistician @IQVIA

Role Description

The Global Biostatistics (Data Sciences, Safety & Medical) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.

As a Statistical Scientist, you will:

• Have access to cutting-edge, in-house technology.
• Work on global projects across a variety of therapeutic areas.
• Lead complex studies and submissions.
• Develop protocols, review case report forms (CRFs), and develop analysis plans.
• Provide input or write specifications for tables and analysis files.
• Communicate with clients regarding study protocol or statistical analysis issues.
• Interpret analyses and write statistical sections of study reports.
• Control costs and maximize revenue recognition.
• Run meetings, provide timeline updates, and assess resource needs.

Qualifications

• BS degree with 7 years of experience or MS degree with 5 years of experience OR equivalent experience.
• Strong knowledge of complex statistical methods that apply to applicable clinical trials.
• Experience in Early Clinical Development phases with Pharmacokinetic/Pharmacodynamic endpoints preferred.
• Strong working knowledge of SAS and CDISC SDTM and ADaM.
• Ability to effectively manage multiple tasks and projects.
• Ability to communicate and explain statistics.

Requirements

• Strong knowledge of complex statistical methods.
• Experience in Early Clinical Development phases preferred.
• Strong working knowledge of SAS and CDISC SDTM and ADaM.

Benefits

• Global exposure.
• Variety of therapeutic areas.
• Collaborative and supportive team environment.
• Access to cutting-edge in-house technology.
• Excellent career development and progression opportunities.
• Work-Life Balance.