Senior Scientist, Statistical Programming

Laboratory Animal Management Association

Rahway, New Jersey, United States
$114,700.00 to $180,500.00; bonus/equity: annual b...
Hybrid
Sas or r programming experience
Business analyst (ba) experience
Reporting processes (sops) and regulatory requirements
Support the centralized management of technology, platforms, inspections, and related process and training for the global Statistical Programming organization to ensure it operates in compliance with departmental and company SOPs, regulatory requirements, and standards

Job Summary

  • Support the centralized management of technology, platforms, inspections, and related process and training for the global Statistical Programming organization to ensure it operates in compliance with departmental and company SOPs, regulatory requirements, and standards.
  • Drive compliance initiatives, change management and communication, and support audit and inspections Center of Excellence with audits, inspections and CAPA management.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and we offer a comprehensive package of benefits.

Matching Summary

Support the centralized management of technology, platforms, inspections, and related process and training for the global Statistical Programming organization to ensure it operates in compliance with departmental and company SOPs, regulatory requirements, and standards.

Salary

$114,700.00 to $180,500.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • SAS or R programming experience
  • Business Analyst (BA) experience
  • reporting processes (SOPs) and regulatory requirements
  • Statistical, Clinical, Medical Monitoring concepts
  • drug/vaccine development
  • project leader
  • deliverable quality and process compliance

Nice-to-have

  • work across cultures and geographies
  • anticipate stakeholder requirements
  • focus on customers
  • inclusive environment
  • respectfully challenge thinking

Key Requirements

  • Master’s degree + 2 years clinical trial experience + 3 years SAS/R
  • Bachelor’s degree + 5 years clinical trial experience + 3 years SAS/R
  • 21 CFR Part 11, ICH GCPs knowledge
  • SDLC understanding
  • pharmaceutical industry experience

Work Rights

Not specified

Tailored Resume

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