Sr. Scientist, Clin. Operations (hybrid)

Mdcrecruiting

Base: $117,000.00 - $184,200.00; bonus/equity: eli...
Hybrid
Clinical trial operational management
Project planning and management
Clinical research regulatory knowledge
This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof as part of a global, cross-functional team

Job Summary

  • This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof as part of a global, cross-functional team.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and will receive a comprehensive benefits package including medical, dental, vision, retirement, paid holidays, vacation, and sick days.
  • The company embraces diversity and inclusion, encouraging colleagues to challenge thinking respectfully and approach problems collectively in an inclusive environment.

Matching Summary

This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof as part of a global, cross-functional team.

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Clinical trial operational management
  • Project planning and management
  • Clinical research regulatory knowledge
  • Timeline management and risk mitigation
  • Stakeholder collaboration and communication
  • Hybrid work model
  • Clinical trial team leadership

Nice-to-have

  • Problem solving and conflict resolution
  • Cross-functional global team experience
  • Experience with immunology clinical trials
  • Experience with imaging and biomarker management
  • Strong presentation and writing skills
  • Inclusive and diverse work environment

Key Requirements

  • Bachelor's Degree plus 5 years experience or Master's Degree plus 3 years experience or PhD/PharmD
  • Experience in pharmaceutical or clinical drug development
  • Knowledge of GCP and ICH guidelines
  • US and Puerto Rico residency required
  • 10% travel availability

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter