Programmer Analyst or Senior Programmer Analyst

Biostatistical Consulting Inc.; Lexington (MA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Disability insurance

FSA

401(k) with match

Annual bonus

Professional development

Private office

Onsite fitness center

Job summary

Biostatistical Consulting Inc. in Lexington, MA seeks a SAS Programmer Analyst to design and run SAS programs for clinical trial data, producing tables, listings, and figures for regulatory submissions.

This role emphasizes quality, accuracy, and working with a cross-functional team in a fast-paced setting. The candidate should have an MS/MA in statistics or biostatistics and practical SAS programming experience in clinical trials, with strong communication skills and ability to manage multiple

Qualifications

• MS/MA in statistics or biostatistics required.
• At least 1 year SAS programming in clinical trials for Programmer Analyst or 3+ years for Senior Programmer Analyst.
• Excellent knowledge of SAS and ability to produce tables, listings, and figures for clinical trials.

Responsibilities

• Develop SAS programs to analyze clinical trial data and produce tables, listings, and figures for FDA/EMA submissions.
• Validate SAS programs and derived datasets for quality and reproducibility.
• Prepare documentation for SAS programs.

Skills

SAS programming

Clinical trials

TablesListingsFigures

Therapeutic areas

Communication skills

Time management

Team collaboration

Meeting timelines

Education

MS/MA in statistics or biostatistics

Tools

SAS

Job description

BCI provides biostatistical and programming services to the pharmaceutical, biotechnology, and medical device industries. Most of our work is in the design and analysis of clinical trials, although we can also design and analyze epidemiology studies and patient registries. BCI employs a select group of biostatisticians and statistical programmers, all of whom have advanced degrees and whose substantial experience spans Phase 1 to Phase 4 clinical trials and a broad range of therapeutic areas. This position requires you to be in office in Lexington, MA.

Qualifications:

Education: MS/MA in statistics or biostatistics

Professional experience:

• Programmer Analyst: Prefer at least 1 year of SAS programming experience in clinical trials in industry (pharmaceutical, biotechnology or medical device) or in academia/medical center.

Or

• Senior Programmer Analyst: Minimum of 3 years of SAS programming experience as above.

Other requirements:

• Excellent knowledge of SAS
• Experience programming of tables, listings, and figures for clinical trials
• Experience with multiple therapeutic areas
• Ability to produce work of the highest quality
• Ability to work on multiple projects simultaneously
• Ability to meet timelines
• Ability to work well with project team and clients
• Excellent oral and written communication skills

Responsibilities:

• Develop SAS programs to analyze clinical trial data and to produce tables, listings, and figures, typically for submission to FDA or European regulatory authority
• Develop SAS programs to validate programs to analyze clinical trial data and to produce tables, listings, and figures
• Develop SAS programs to produce or validate derived datasets
• Develop SAS programs to produce or validate tables, listings, and figures for ISE and ISS
• Produce documentation for SAS programs

In addition to vacation, holiday and sick time, benefits include medical, dental, vision and disability insurances, FSA, 401(k) retirement plan with matching and profit sharing, annual bonus, professional development training, private office, and onsite fitness center.

• H-1B SPONSORSHIP CAN BE PROVIDED, IF NEEDED