Job description

DataTek is a professionally run global IT consulting firm that defines , designs and delivers technology. We provide information technology solutions for our Fortune 500 companies in the USA and around the world. Our specializations span Information Technology Consulting, Software Developing, Staff Augmentation, Project Outsourcing and Direct Placement. A blend of Experience, Dynamism and Commitment, our Board and Management team delivers services that work for our clients and builds strategic long-term client relationships.

Biostatistician

Job Description:

Participate in Clinical trial Study Team meetings for assigned clinical trial studies; Responsible within the Clinical Study Team for the quality, accuracy and timely completion of assigned tasks; Work on analysis of clinical trials; Analyze and interpret data from individual clinical trials; Perform clinical trial analyses by pooling data from several clinical trial studies; Assist in the writing of comprehensive clinical trial reports and creative table, listing and figure shells; Prepare project summaries for weekly/monthly status meetings; Maintain state of the art statistical applications in clinical trial research; Responsible for data processing for accurate relocation, formatting, generating and transmitting required data; Prepare statistical contribution to Integrated Study Report.

Job Responsibilities:

• Support multiple clinical trial studies independently
• Help create SAP (Statistical Analysis Plan) under principal biostatistician guidance
• Contribute to the development and maintenance of methods and procedures based on client requirement
• Assist Sr. statistician to generate shells for Tables, Listing and Figures (TLF)
• Provide programming support for clinical trial data reporting and regulatory submissions
• Develop and execute statistical analysis of clinical trial data under the general guidance of Sr. statisticians
• Validate SAS programs that produce tables, figures and datasets that summarize results of clinical trials.
• Demonstrate SAS programming skills
• Participate meeting in clinical trial team, functional project team and medical team.
• Provides timely and effective communication with programming leads, Sr. biostatisticians and medical teams including clinical technical writers.
• Perform data and statistical analysis using SAS language, procedures and Macros.

Education and Experience:

• MS/PhD degree S.T.E.M majors, but prefer in statistics, biostatistics, applied statistics, mathematics or biology
• Minimum one year experience including academical experience required or equivalent training

Knowledge, Skills and Abilities:

• Strong SAS programming skills and understand R is plus
• Strong knowledge of statistical principles and strong statistical skills
• Excellent written and verbal communications skills
• Good organizational skills with the ability to adapt and adjust to changing priorities
• Positive attitude and the ability to work well with others

Benefit:

• Holiday and Vacation pay
• Medical, Dental, Vision and Life insurance
• 401K Retirement plan
• Sponsor H-1B and GC, but prefer permanent resident and US citizenship

Job Type: Full-time

Schedule:

• Monday to Friday

Work Location: Remote

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