Biostatistician

Brightech is a leading CRO that specializes in complex, value-add biostatistics, programming, and clinical data management services. Brightech, an Everest Clinical Research Company, has earned a highly-regarded reputation as a critical partner for some of the world’s largest pharmaceutical and biotech companies. Our Brightech Taipei, Taiwan office has an opening for Biostatistician candidates at all levels.

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Little Falls (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan, Republic of China.

Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.

Responsibilities Include

• Participates in study design; sample size estimation, protocol writing

• Develop Statistical Analysis Plan and output shells • Create ADaM specifications.

• Perform validation on statistical analysis and QC output (Tables/Listing/Figures).

• Participates in clinical trial project meetings.

• Applies statistical methodology to clinical trials.

• Acts as a project statistician interacting with clients and co-workers.

• May present and interpret study results.

• May provide consultation to clients regarding statistical and mathematical questions pertaining to the design and interpretation of clinical studies.

• Performs additional tasks as assigned.

Qualification and Experience:

A Master’s degree plus at least 2 years highly relevant experience, with demonstrated ability and sustained performance.