Clinical Scientist

ICON plcMontreal, QC
Remote

About The Position

ICON plc is a world-leading healthcare intelligence and clinical research organization. The Clinical Scientist will assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management. This role may involve supporting a single study or multiple studies, or even leading a study with limited scope (e.g., Survival Follow-up). The Clinical Scientist will also interact with internal and external stakeholders such as study sites and committees to support clinical study objectives. ICON is committed to fostering an inclusive environment, driving innovation and excellence, and shaping the future of clinical development. The company is an award-winning workplace dedicated to making a difference in patients' lives by delivering new medicines and medical devices, while also conducting business sustainably and supporting local communities.

Requirements

  • BS/BA/MS/PhD in Life Sciences with 2+ yrs relevant career experience
  • If no degree in Life Sciences, must have significant experience in clinical development (>5 years)
  • At least 1 year of medical monitoring required
  • Demonstrated oral and written communication skills
  • Excel and PP experience required
  • Ability to travel up to 15% (might include international travel)
  • Legally authorized to work in the United States and/or Canada

Nice To Haves

  • Pharmaceutical experience beneficial
  • Respiratory (specifically COPD) experience highly preferred
  • 2 years medical monitoring experience highly preferred
  • ePro experience a plus

Responsibilities

  • Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management
  • May support a single study or multiple studies
  • May lead a study with limited scope (e.g., Survival Follow-up)
  • May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Benefits

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume

What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Number of Employees

5,001-10,000 employees

© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service