Senior Clinical Scientist

ICON plc

United States
Clinical point of contact
Medical monitoring plan development
Protocol clarification letters
May lead or support a study or studies, depending on size/complexity, and if lead, accountable for the clinical/scientific execution of the protocol

Job Summary

  • May lead or support a study or studies, depending on size/complexity, and if lead, accountable for the clinical/scientific execution of the protocol.
  • Responsible for trial design and endpoint development in collaboration with CD Leads the Medical Monitoring (MM) team in performing MM activities.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

May lead or support a study or studies, depending on size/complexity, and if lead, accountable for the clinical/scientific execution of the protocol.

Skills & Requirements

Must-have

  • Clinical point of contact
  • Medical Monitoring Plan development
  • Protocol clarification letters
  • Investigator Meeting presentations
  • Protocol deviation classifications

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Mentoring other Clinical Scientists

Key Requirements

  • BS/BA in Life Sciences with 7+ yrs experience
  • MS/PhD in Life Sciences with 5+ years experience
  • >11 years clinical development experience
  • Minimum 2 years lead CS experience
  • Medical monitoring experience required
  • Legally authorized to work in Canada or US

Work Rights

Legally authorized to work

Tailored Resume

Cover Letter