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Clinical Scientist - ONC/ID/Vac/Neuro/Cardio/IMM

ICON plc

Blue Bell, SD; Any City, CanadaRemotePosted 26 days ago
Full TimeMid LevelClinical DevelopmentCRO
Original posting ↗

Summary

Position based remote in US or Canada

Job description

What you will be doing:

  • 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

What you need to have:

Educational 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)

Minimum Years of Experience

  • Pharmaceutical experience beneficial but not required
  • Experience in Oncology, ID/Vac, Neuro, Cardio, and/or Immunology required
  • 2 years medical monitoring experience highly preferred
  • ePro experience a plus
  • Demonstrated oral and written communication skills
  • Excel and PP experience required
  • Ability to travel up to 15% (might include international travel)
  • To qualify, applicants must be legally authorized to work in the United States and/or Canada, and should not require, now or in the future, sponsorship for employment visa status

Position based remote in US or Canada

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)
  • Experience in Oncology, ID/Vac, Neuro, Cardio, and/or Immunology required
  • 2 years medical monitoring experience highly preferred
  • ePro experience a plus
  • Demonstrated oral and written communication skills
  • Excel and PP experience required
  • Ability to travel up to 15% (might include international travel)
  • To qualify, applicants must be legally authorized to work in the United States and/or Canada, and should not require, now or in the future, sponsorship for employment visa status

Benefits

  • Competitive base salary
  • Performance related incentives
  • Medical, Dental & Vision
  • Retirement and pension plans
  • Life assurance and disability
  • Employee assistance programmes
  • Wellbeing resources
  • Learning and development opportunities

Company overview

ICON plc is a global leader in clinical research and healthcare intelligence, founded in Dublin, Ireland in 1990. As one of the world's largest contract research organizations (CROs), ICON provides comprehensive outsourced development services to pharmaceutical, biotechnology, and medical device companies worldwide. The company operates in 55 countries with approximately 41,900 employees, offering end-to-end solutions that span the entire product development lifecycle. ICON's service portfolio includes clinical research services, adaptive trials, biosimilars, commercialization and outcomes consulting, medical imaging, laboratory services, and strategic support for traditional and digital health technologies. The company specializes in therapeutic areas such as oncology, cardiovascular diseases, central nervous system disorders, rare diseases, and women's health. With its 2021 acquisition of PRA Health Sciences, ICON significantly expanded its capabilities and market position, becoming a dominant force in the global CRO industry. The company is publicly traded on NASDAQ under the ticker ICLR and reported $8.28 billion in revenue for 2024.

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