Clinical Scientist - Oncology

ICON; United States; Remote; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive base salary

Health, dental, and vision coverage

Retirement plans

Life assurance

Employee assistance programs

Learning and development opportunities

Job summary

ICON Strategic Solutions is seeking a clinical monitoring professional to support sponsor-dedicated studies. You will assist the CS Protocol Lead with medical monitoring, data reconciliation, and meeting materials, while coordinating with study sites and internal teams.

The role may lead a study with limited scope, requires travel up to 15%, and demands strong communication skills, Excel and PowerPoint proficiency, and work authorization for the United States and/or Canada.

Qualifications

• Bachelor's/Master's/PhD in Life Sciences with 2+ years of clinical experience.
• If no Life Sciences degree, extensive clinical development experience (>5 years) is required.

Responsibilities

• Assist the CS Protocol Lead and study team with clinical/scientific conduct of clinical studies including adjudication support, medical monitoring, and data reconciliation.
• Prepare meeting materials, manage protocol deviations, and support single or multiple studies as needed.
• May lead a study with limited scope and interact with study sites and committees to support objectives.

Skills

Oral and written communication

Excel

PowerPoint

Travel availability

Education

Life Sciences degree (BS/BA/MS/PhD) with 2+ years relevant experience

Significant clinical development experience (>5 years) if no Life Sciences degree

Tools

ePro

Job description

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.

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.