Description
As a Clinical Scientist - Oncology at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
You will assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, and protocol deviation management.
Responsibilities:
- Assist the CS Protocol Lead and study team with clinical/scientific conduct of clinical studies
- Support a single study or multiple studies
- Lead a study with limited scope (e.g., Survival Follow-up)
- Interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives
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)
- 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)
Rewards & Benefits:
- 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