Scientist, Clinical Research Operations - Ophthalmology - Hybrid

Imsapharma Com Ar

Base: $87,300.00 - $137,400.00; bonus/equity: elig...
Hybrid
Gcp and ich regulatory requirements
Clinical study data monitoring
Protocol and study materials development
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 training materials.
  • The company offers a comprehensive package of benefits including medical, dental, vision, retirement, paid holidays, vacation, and compassionate and sick days.

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: Comprehensive package including medical, dental, vision, retirement, paid holidays, vacation, and sick days

Skills & Requirements

Must-have

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

Nice-to-have

  • proactive approach to study goals
  • respectfully challenge thinking
  • drive breakthrough innovation

Key Requirements

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

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter