Scientist, Clinical Research Operations - Ophthalmology - Hybrid

microsatsystems.biz

Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid
Gcp and ich regulatory requirements
Clinical trial data interpretation
Cross-functional collaboration
This position contributes to the scientific planning and execution of one or more clinical trials, assisting the Lead Clinical Scientist and study team with the scientific conduct of clinical studies

Job Summary

  • This position contributes to the scientific planning and execution of one or more clinical trials, assisting the Lead Clinical Scientist and study team with the scientific conduct of clinical studies.
  • Responsibilities include medical monitoring, lab specimen tracking, adjudication support, and supporting the development of protocols, ICF documents, and data management deliverables.
  • The role offers the opportunity to develop leadership, technical skills, and scientific acumen as part of a global, cross-functional team.

Matching Summary

This position contributes to the scientific planning and execution of one or more clinical trials, assisting the Lead Clinical Scientist and study team with the scientific conduct of clinical studies.

Salary

Base: $87,300.00 - $137,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • GCP and ICH regulatory requirements
  • clinical trial data interpretation
  • cross-functional collaboration
  • protocol and study material development
  • clinical study data monitoring

Nice-to-have

  • proactive approach to study goals
  • problem solving and conflict resolution
  • leadership and technical skill development

Key Requirements

  • Bachelor's Degree +2 years experience OR Master's Degree +1 year experience
  • Ophthalmology experience required
  • Life sciences degree preferred

Work Rights

Not specified

Tailored Resume

Cover Letter