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indeed

Sr Programmer Analyst II

Thermo Fisher Scientific
Maharashtra, IND
Full-time
Onsite
Discovered 1 months ago
SASstatistical programmingclinical programmingbioinformaticsclinical trialsrelational databases

Full Job Posting

Work Schedule

  • Standard Monday through Friday work schedule.

Work Environment

  • Work is performed in an office environment.
  • Occasional travel to site locations and occasional domestic and international travel may be required.

Role Overview

The Senior Programmer Analyst performs advanced bioinformatics programming activities supporting the statistical and computational requirements of research projects.

The role works independently as lead programmer on selected moderately complex studies and may support more complex studies under a lead programmer.

The role provides training and guidance to junior team members.

Programming and Bioinformatics Activities

  • Create, execute, maintain, and validate programs that transfer data across multiple data management systems or operating systems.
  • Combine data from varied sources and structures and generate and store summary data.
  • Generate reports or combine multiple databases.
  • Validate SAS programs that generate listings, tables, and figures.

Study Leadership and Quality

  • Act as lead programmer on selected studies of moderate complexity and work with project leaders and client representatives.
  • Assess project goals and timelines and contribute leadership to multidisciplinary clinical trials teams.
  • Manage and document assignments, maintain awareness of contractual obligations, and provide statistical programming quality control review.

Training and Departmental Support

  • Develop programming, clinical trials, and pharmaceutical industry knowledge and provide training and mentoring.
  • Support conferences, department meetings, training materials, departmental documents, policies, working practice documents, SOPs, and bidding activities.

Education and Experience Requirements

  • Bachelor’s or Master’s degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field, or an equivalent relevant academic or vocational qualification.
  • At least 6 years of relevant experience in statistical programming, clinical programming, or a related field.
  • Experience supporting clinical trials in the pharmaceutical, biotechnology, or CRO industry.
  • Strong SAS programming experience.

Knowledge, Skills, and Abilities

  • Understanding of programming languages, relational database structures, complex data systems, and biostatistical metrics.
  • Strong attention to detail, problem-solving, innovation, written and verbal communication, and collaboration skills.
  • Ability to manage multiple assignments, adapt to changing priorities, and train and mentor others.
  • Proficiency in English.

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