Syneos Health
Syneos Health
Syneos Health is a fully integrated biopharmaceutical solutions organization that helps clients move therapies from clinical development to commercial delivery. Its teams combine clinical, medical affairs, commercial, technology, and market insights to address changing healthcare needs and support the development and launch of important treatments worldwide.

Senior Statistical Programmer (Remote - India)

Lead SAS-based programming for clinical trial outputs at Syneos Health, including datasets, tables, listings, and graphs. Coordinate validation, documentation, team leadership, and sponsor deliverables across multiple projects.

Description

  • Create custom SAS or other software programs that produce summary tables, data listings, graphs, and derived datasets from statistical analysis plans and programming specifications.
  • Verify that programming outputs satisfy applicable quality standards and project requirements.
  • Conduct validation programming and resolve discrepancies with programmers, biostatisticians, and project team members.
  • Keep project documentation, testing, verification, and quality-control records complete and current for inspection readiness.
  • Coordinate schedules and priorities across multiple projects while adjusting workloads as timelines change.
  • Define specifications for datasets and outputs and identify potential programming issues in advance.
  • Organize and lead internal meetings, circulate information and minutes, and track action items to completion.
  • Direct statistical programming activities and oversee other programming staff.
  • Track progress against programming deliverables.
  • Review Statistical Analysis Plans, mock shells, programming specifications, annotated CRFs, and SAS database designs.
  • Represent statistical programming in sponsor, kickoff, and bid defense meetings.
  • Support the development of programming personnel through training, work reviews, feedback, and process guidance.
  • Transfer deliverables and complete other assigned work-related duties.

Requirements

  • Bachelor’s degree, preferably in a scientific or statistical field, or an equivalent combination of education and demonstrated programming experience.
  • Extensive experience programming in SAS or other required software, preferably within a clinical trial setting.
  • Strong written and verbal communication skills.
  • Professional proficiency in reading, writing, speaking, and understanding English.
  • Ability to create dataset and output specifications of any complexity in line with statistical and sponsor requirements.
  • Willingness to undertake minimal travel if required.

Benefits

  • Opportunities for career development and progression.
  • Supportive, engaged line management.
  • Training in technical and therapeutic areas.
  • Peer recognition programs.
  • Total rewards program.
  • Inclusive workplace culture.
  • Reasonable accommodations, where appropriate, for employees or applicants with disabilities.

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