To be successful in this role, you will need to have demonstrate all of the below:
• MPH, MSc or PhD in Biostatistics or related field
• 3 - 5 years of experience in a similar role, ideally from CRO/Pharma industry
• 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
• Strong consulting and client engagement skills
• Ability to meet short deadlines with high quality deliverables
• Strong written and verbal communication skills
• Fluency in English (spoken and written)
• Working knowledge of relevant Data Standards (such as Clinical Data Interchange Standards Consortium CDISC/ADaM)

We would also prefer you to have:

• Proven ability to manage a team
• Prior experience working in a consultancy, CRO, or life sciences company
• Knowledge of data needs of pharmaceutical clients
• History of successful project management, including client negotiations, contracting experience and scope management
• Expertise in heath informatics

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.

Work Hours: 8 60 Postgraduate Degree