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Clinical Scientist

Role overview

Qualifications

  • BS/BA/MS/PhD in Life Sciences with 2+ yrs relevant career experience
  • Experience in Oncology required
  • 2 years medical monitoring experience highly preferred
  • Demonstrated oral and written communication skills

Responsibilities

  • Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies
  • May support a single study or multiple studies
  • May lead a study with limited scope
  • May interact with internal and external stakeholders in support of clinical study objectives

Key facts

Hard skills

Other skills

  • Microsoft Excel
  • Microsoft PowerPoint
  • Communication

About the company

ICON plc logo

ICON plc

Contract Research Organizations (CRO)

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

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 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.


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Marcus Rivera

Chief Revenue Officer

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