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Sr. Clinical Informatics Consultant - (Remote)

Biostatistician
REMOTE, New York, US
  • Added - 21/09/2026
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Pay Rate Low: $75 | Pay Rate High: $90

Our client is seeking a Senior Biometrics Informatics Consultant to lead the evaluation, selection, and implementation of a new Statistical Computing Environment supporting clinical development.

Title: Senior Biometrics Informatics Consultant/SCE Implementation Lead (Remote)
Pay Rate: $75–$90/hr ( + Benefits)
Contract Duration: 12 months
Location: US based, Occasional onsite support in San Francisco is required (1-2x a month)

Position Overview
This consultant will partner closely with Clinical Data Management, Statistical Programming, Biostatistics, and Clinical Pharmacology teams to assess current-state capabilities, define business and technical requirements, evaluate potential vendors, and lead the implementation and validation of the selected solution.
Key Responsibilities

  • Lead requirements gathering and current-state assessment for a new Statistical Computing Environment.
  • Evaluate potential SCE vendors, including coordinating vendor demonstrations, technical assessments, pilots, and selection activities.
  • Develop system/interface maps and vendor evaluation scorecards to support the selection process.
  • Partner with internal stakeholders to develop and evaluate RFPs and support vendor negotiations and purchasing activities.
  • Lead the technical configuration, implementation, integration, and validation of the selected SCE.
  • Collaborate with Clinical Data Management, Statistical Programming, Biostatistics, and Clinical Pharmacology teams to ensure the solution meets clinical development needs.
  • Support clinical programming workflows across SAS and Python environments.
  • Serve as the technical subject-matter expert throughout implementation, validation, user acceptance, and transition to ongoing operations.
  • Partner with internal teams and external vendors to troubleshoot technical and workflow challenges.
  • Ensure implementation activities align with GxP requirements, computer system validation expectations, and SOP-driven processes.
  • Support successful handoff of the new environment to internal stakeholders and operational teams.
Required Qualifications
  • 5+ years of experience supporting or leading the implementation of Statistical Computing Environments within drug development.
  • Demonstrated experience with vendor evaluation, selection, and implementation of validated systems within a biotech or pharmaceutical environment.
  • Must be Authorized to work in the United States without sponsorship.
  • Strong understanding of SAS and R programming practices within clinical development.
  • Experience gathering and translating requirements from Biostatistics, Statistical Programming, Clinical Pharmacology, and/or Clinical Data Management teams.
  • Experience working within GxP-regulated environments, including computer system validation and SOP-driven processes.
  • Strong project coordination, stakeholder management, and communication skills.
  • Ability to work effectively across technical, clinical, and vendor teams.
Preferred Qualifications
  • Experience with Databricks.
  • Knowledge of clinical data standards.
  • Experience with Git/Git-based development workflows.
  • Experience with AI-assisted SAS or R coding.
  • Experience supporting modernization or migration from legacy statistical computing platforms.

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