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

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 to read more about the benefits ICON offers.