Biostatistician

About Cetas Healthcare: Cetas Healthcare is a global firm specializing in customer insights and strategy for the medical devices industry. With offices in Singapore, Mumbai, Chicago, New York, Norway, and Brazil, Cetas Healthcare works closely with top Med Tech companies such as GE Healthcare, Boston Scientific, J&J, Medtronic, Philips, Roche Diagnostics, etc. Cetas Healthcare is a preferred market research vendor for many of our Med Tech clients. We are preferred primarily for expertise in MedTech industry AND for the capability to design and execute complex market research studies in multiple countries.

The Biostatistician will work independently but as part of a larger team supporting client clinical trials. This role will work directly with client points of contact to review statistical reporting, provide statistical analysis and various adhoc tasks as statistician.

Job Requirements

Review of statistical and safety reports

Perform statistical analysis

Lead protocol development work including experimental design, randomization, sample size calculation, statistical methods, defining study objectives and parameters.

Coordinate and approve the statistical section of the Clinical Study Report (CSR) written by Biostatistics staff and collaborate with Medical Writer in preparing the integrated CSR as needed.

Experience in multiple therapeutic areas and across multiple phases of clinical trials

Experience in writing Statistical Analysis Plan including mock TLF s, providing input to study documents like protocol, CRF, database designing and CSR

Experience in advance statistical techniques and sample size calculation

Experience in writing statistical report

Ability to work independently with least/no supervision & work effectively in a team environment.

Exploratory analysis

Publications, manuscript review, writing

Adhoc requests

Participation at study level to guide programmers

Requirements

Job Qualifications

Master s degree in Statistics/Biostatistics or other subject with high statistical content with 5 years of post-graduate statistical experience in the pharmaceutical industry or medical research or Doctoral degree in Statistics/Biostatistics or other subject with high statistical content with 2 years of post-graduate statistical experience

Designing, analyzing and/or reporting clinical trials within Pharmaceutical/Biotechnology/Public Health setting in Industry, Government or Academia

Strong fundamentals of Project Planning

Communication of statistical information (written and oral)

Strong understanding of statistical concepts related to the design and conduct of clinical studies

Strong ability to apply statistics in the analysis of clinical trials

Excellent oral and written English communication skills

Job Qualifications Master s degree in Statistics/Biostatistics or other subject with high statistical content with 5 years of post-graduate statistical experience in the pharmaceutical industry or medical research or Doctoral degree in Statistics/Biostatistics or other subject with high statistical content with 2 years of post-graduate statistical experience Designing, analyzing and/or reporting clinical trials within Pharmaceutical/Biotechnology/Public Health setting in Industry, Government or Academia Strong fundamentals of Project Planning Communication of statistical information (written and oral) Strong understanding of statistical concepts related to the design and conduct of clinical studies Strong ability to apply statistics in the analysis of clinical trials Excellent oral and written English communication skills