Job Description Summary As Biostatistician you will work closely with the Senior Director of Statistics to provide statistical services for analysis, reporting, and statistical programming specific activities. This may include development of statistical analysis plan, randomization schedule, conducting statistical analyses, validating programming and reporting output, and developing statistical analysis report.

The role will also involve some CRO management and working with the Global Head of Biometrics and the Senior Director to ensure delivery of statistical deliverables with vendor partners is on time.

Job Description Roles and Responsibilities

• Provide statistical analysis services related to clinical trials and other studies including observational studies relating to imaging modalities and drug agents.
  
• Work with the vendor to define analysis data specifications, SAP development, evaluating acceptability of statistical methods (with support from the Director of statistics).
• Interact with programmers and other statisticians and other relevant personnel.
• Review the statistical analysis plan and provide input into the study protocol (with support from the Director of Biostatistics).
• Collaborate with Data managers and medical writers to write and review (statistical) sections of the final study reports and protocols
• Develop SAS programs to generate analysis datasets, and trial specific reporting including but not limited to tables, listings, graphs, queries, and patient profile reports.

Required Qualifications

• Master in Statistics or Mathematics (emphasis in Statistics)
• Experience in Pharmaceutical/Biotechnology industry or equivalent statistical consulting and statistical programming role
• Excellent verbal and written communication skills in English

Desired Characteristics

• Strong experience in various SAS software modules including SAS/STAT, and SAS/Graph.
• Experience in statistical support of clinical trials Knowledge of ICH guidelines and other guidelines such as GCP, and 21 CFR Part 11 from different regulatory agencies including FDA, and EMEA.
• Experience in conducting and writing statistical analyses reports using SAS for various trial level deliverables
• Excellent team player

Eligibility requirements

• A good level of English

Inclusion and Diversity

GE Healthcare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

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Additional Information Relocation Assistance Provided: No