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

  • Canada, United States
  • Remote
  • Posted Oct 9, 2026
  • 1 position

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Employment type
Full-time
Experience level
Mid-level · 2+ years
Minimum education
Bachelor’s degree
Posting language
English
Working hours
40 hours per week

Job summary

The Clinical Scientist assists the Protocol Lead with the clinical and scientific conduct of studies, including medical monitoring and protocol deviation management. They also facilitate communication with internal and external stakeholders to ensure clinical study objectives are met.

Job details

Clinical Scientist - Oncology - Home Based (US or Canada) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. 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 Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply

What you’ll do

The Clinical Scientist assists the Protocol Lead with the clinical and scientific conduct of studies, including medical monitoring and protocol deviation management. They also facilitate communication with internal and external stakeholders to ensure clinical study objectives are met.

Requirements

Candidates must hold a degree in Life Sciences with at least 2 years of relevant experience, or significant clinical development experience if the degree is in another field. Proficiency in Oncology, ID/Vac, Neuro, Cardio, or Immunology is required, along with strong communication skills and experience with Excel and PowerPoint.

Benefits

  • Competitive base salary
  • Performance related incentives
  • Medical coverage
  • Dental coverage
  • Vision coverage
  • Retirement plans
  • Pension plans
  • Life assurance
  • Disability coverage
  • Employee assistance programmes
  • Wellbeing resources
  • Learning and development opportunities

Listed skills

  • Microsoft Excel · Preferred
  • Stakeholder Management · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

  • Clinical research
  • Medical monitoring
  • Protocol deviation management
  • Imaging data reconciliation
  • Adjudication support
  • Oncology
  • Immunology
  • Neurology
  • Cardiology
  • Infectious disease
  • Vaccinology
  • Clinical study conduct
  • Stakeholder management
  • Microsoft Excel
  • Microsoft PowerPoint
  • ePro
  • Deviation Management
  • Medical Monitoring
  • Adjudication
  • Reconciliation
  • Pre-Clinical Development
  • Clinical Trials
  • Communication
  • Electronic Patient-Reported Outcome
  • Life Sciences
  • Pharmaceuticals

Job areas

  • Healthcare
  • Science & Research
  • Consulting
  • Clinical Scientist
  • Medical Research Scientist
  • Biologists, Botanists, Zoologists and Related Professionals
  • Medical Scientists, Except Epidemiologists

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