Clinical Scientist - Oncology - Home Based (US or Canada)
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 CanadaRewards & BenefitsICON 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.
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