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Senior Clinical Programmer

Senior Clinical Programmer

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Senior Clinical Programmer

  • Location:

    New York

  • Sector:

    Technical Operations - Pharma

  • Contact:

    Anjali Kalairajah

  • Salary:

    Negotiable

  • Job type:

    Permanent - full time

  • Contact email:

    Anjali.Kalairajah@msipharma.com

  • Job ref:

    VR/04559_1707132823

  • Published:

    23 days ago

  • Duration:

    ongoing

  • Startdate:

    ASAP

The Clinical Statistician will join an exciting, market leading, global pharmaceutical company with a strong pipeline of 80+ assets that are reinforcing their clinical data team. The company prioritizes patient safety, innovation and global reach. This role will support the clinical drug research and development process by providing strategic planning and execution, including data transformation and all aspects of data analysis related to clinical projects.

Benefits

Highly competitive salary & benefits package (including pension scheme, 401k contribution, medical insurance, 20+ days PTO etc)
Hybrid Working
Great opportunity for career development
Prioritising Work/Life balance

Duties & Responsibilities

  • Accountable for transforming, analyzing and reporting phase I-IV clinical trials.
  • SAS programming
  • Ensure data transformation and analysis specifications
  • Supporting the clinical drug development process as a BDS Product Owner on the level of projects/assets.

Requirements

  • Bachelor of Science (BSc) in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.) OR
  • Master of Science (MSc) in Statistics, Mathematics, Computer Science or related field (Psychology, Data Science, Finance, etc.)
  • ADaM data set creation
  • Working to CDISC standards
  • SAS programming
  • Strong statistical knowledge
  • Project lead experience.
  • Demonstrated advanced knowledge in planning, transforming, analyzing, interpreting, and reporting data in clinical trials or data from other sources in clinical research and development.
  • Ability to lead and facilitate meetings.
  • Experience working cross functionally
  • Understand and implement International regulations and guidelines for good clinical and statistical practice from all ICH regions including statistical methodology, for TA-related disease areas, and Processes and SOPs that govern clinical development

Job Type: Full-time

Benefits:

  • 401(k)
  • Dental insurance
  • Health insurance
  • Paid time off
  • Relocation assistance
  • Retirement plan
  • Vision insurance

Compensation package:

  • Bonus opportunities