Project Manager B: Protocol Development, Clinical Statistics And Data Analyses

University of Pennsylvania

Philadelphia, Pennsylvania, US
Base: $66,000.00 - $81,441.00 annual rate; bonus/e...
Clinical research protocol design
Sas and stata statistical programming
Regulatory compliance gcp standards
This role involves strategic planning and day-to-day management of complex clinical trials with internal and external collaborators at the University of Pennsylvania

Job Summary

  • This role involves strategic planning and day-to-day management of complex clinical trials with internal and external collaborators at the University of Pennsylvania.
  • The position requires designing detailed study protocols, analyzing large-scale surgical outcome databases using SAS and Stata, and ensuring regulatory compliance for FDA submissions.
  • Candidates will benefit from a competitive package including excellent healthcare, tuition assistance for employees and families, and generous retirement plans.

Matching Summary

This role involves strategic planning and day-to-day management of complex clinical trials with internal and external collaborators at the University of Pennsylvania.

Salary

Base: $66,000.00 - $81,441.00 Annual Rate; Bonus/Equity: Not specified; Benefits: Comprehensive healthcare, tuition assistance, retirement plans

Skills & Requirements

Must-have

  • Clinical research protocol design
  • SAS and Stata statistical programming
  • Regulatory compliance GCP standards
  • Investigator initiated study management
  • Informed consent form drafting

Nice-to-have

  • Community partner relationship building
  • Mentoring medical residents and fellows
  • Complex database system integration
  • NIH grant application experience
  • Manuscript drafting for peer review

Key Requirements

  • Master of Science degree required
  • 3 to 5 years of clinical research experience
  • Familiarity with GCP regulatory processes

Work Rights

Not specified

Tailored Resume

Cover Letter