Statistical Programmer

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 Statistical Programming 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:

1. Reads and analyzes protocol, statistical analysis plan, CRF and other trial design documents and discusses with other team members such with as biostatisticians and data managers.

2. Develops and debugs simple to complex SAS program in a timely manner

3. Implements statistical analysis plan, data preparation, and data manipulation into SAS programs and macros

4. Create analysis datasets, statistical tables, figures, and listing for clinical trial data.

5. Create CDISC standard datasets (SDTM and ADaM)

6. Participates in the validation of SAS programs and analysis datasets

7. Maintains documentation for SAS programs and validation results

8. Leads and coordinates the programming work for projects involving SAS programming if necessary

9. Coordinates timelines in orders to fulfill the needs of other departments

Qualifications and Experience:

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