Senior Scientist, Statistical Programming

539

Rahway, New Jersey, United States
$114,700.00 to $180,500.00; bonus/equity: annual b...
Hybrid
Sas or r programming experience
Clinical trial environment experience
Business analyst (ba) experience
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.
  • Support the Business System Ownership (BSO) of platforms or applications and corresponding documents and training.
  • We offer a comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits, retirement benefits, 401(k), paid holidays, vacation, and compassionate and sick days.

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: Comprehensive package of benefits

Skills & Requirements

Must-have

  • SAS or R programming experience
  • clinical trial environment experience
  • Business Analyst (BA) experience
  • reporting processes aligned with regulatory requirements
  • Statistical, Clinical, Medical Monitoring concepts
  • drug/vaccine development processes
  • project leader capabilities

Nice-to-have

  • anticipate stakeholder requirements
  • focus on customers
  • work across cultures and geographies
  • effective interpersonal skills
  • negotiate and collaborate effectively

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
  • Business Analyst (BA) experience
  • Knowledge of reporting processes (SOPs) and SDLC
  • Understanding of Statistical, Clinical, Medical Monitoring, Data Management concepts
  • Experience in developing analysis and reporting deliverables

Work Rights

Not specified

Tailored Resume

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