Director Stat. Programming - Sdsqm (hybrid)

Mericalherbs

Rahway, New Jersey, USA
Base: $190,800.00 - $300,300.00; bonus/equity: eli...
Hybrid (3 days on-site, 1 day remote)
Sdtm data deliverables
Cdisc data standards experts
Regulatory guidance and submission standards
Mericalherbs is seeking a Director of Statistical Programming for their Biostatistics and Research Decision Sciences department, based in Rahway, New Jersey. The ideal candidate will have extensive experience in statistical programming within clinical trials, strong leadership skills, and knowledge of regulatory compliance, with a hybrid work model that includes three days on-site

Job Summary

  • The Quantitative Sciences team uses big data to analyze the safety and efficacy claims of our potential medical breakthroughs.
  • The Director is accountable for a team of CDISC data standards experts, sets the strategic and operating direction for the SDSQM SC team, and effectively collaborates with stakeholders at all levels.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and a comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits, retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Matching Summary

Match Score: 85

Mericalherbs is seeking a Director of Statistical Programming for their Biostatistics and Research Decision Sciences department, based in Rahway, New Jersey. The ideal candidate will have extensive experience in statistical programming within clinical trials, strong leadership skills, and knowledge of regulatory compliance, with a hybrid work model that includes three days on-site.

Salary

Base: $190,800.00 - $300,300.00; Bonus/Equity: eligible for annual bonus and long-term incentive; Benefits: comprehensive package of benefits

Skills & Requirements

Must-have

  • SDTM data deliverables
  • CDISC data standards experts
  • regulatory guidance and submission standards
  • clinical trial programming
  • regulatory agency requirements

Nice-to-have

  • strategic thinking and tactical activities
  • championing and driving proficiency
  • process improvement
  • work across cultures and geographies

Key Requirements

  • BS plus 12 years or MS with 10+ years experience
  • 2 years statistical programming experience
  • 7+ years project management experience
  • US and/or worldwide drug or vaccine regulatory application submission experience

Work Rights

Not specified

Tailored Resume

Cover Letter