Biostatistician

Work Your Magic with us! 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Your Role:

Provide statistical expertise and contribution in the conduct of human subjects research during clinical development and life cycle management. 

As a study biostatistician for statistically standard clinical studies and under supervision:  
o    act as Statistical subject matter expert at study team level o provide statistical input for concept sheet/protocol/CRF development (e.g., study design; sample size estimation for the most efficient and practical design; patient randomization; accurate, logical, clear, concise and thorough statistics section; effective CRF specifications to collect data specified in the protocol, ensure blinding/unblinding measure are taken to ensure data integrity) with supervision.  o author medical and statistical supervision plans, write statistical analysis plans including the most appropriate statistical methodology and data presentations and provide specifications for analysis datasets. 
o    perform statistical analyses or validate statistical output as required or able to conduct oversight of vendor for these studies 
o    write comprehensive statistical methods sections for the clinical study report; critically review and coauthor these reports ensuring the accuracy of the statistical interpretation. 
With surpervision, able to effectively perform ad’hoc analysis or project related standard reporting (e.g., DSUR) 
Understand and follow all Global Biostatistics WIs/SOP and relevant Standards as well as any other relevant WIs/SOPs. 

May act as an interface between programming and statistic. The responsibilities include but are not limited to performing complex statistical analyses. With expertise in statistics and programming you be able to transform complex statistical models into programming code and use state-of-the-art modelling techniques to provide solutions. Further,  will supervise CROs and provide advice and technical solutions on programming task and standard macros. Will closely work with the project statisticians and project programmers in addition to clinical and project teams.

Who you are:
• MS in Statistics, Biostatistics or related discipline 
• Fluent in English (written and spoken)

Skills:

•    SAS and R practical and effective knowledge  
•    Ability to develop an understanding of relevant clinical therapeutic areas 
•    Results driven 
•    Collaborative 
•    Act purposefully 

We are an equal opportunity employer that values workforce diversity. We want everyone to be able to bring their best self to work every day which is why equality and inclusion is at the forefront of all our activities. We are dedicated to a policy of non-discrimination in employment on any basis including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!