Remote Clinical Scientist – Oncology & Immunology (US/Canada)

ICON Strategic Solutions; United States; A distancia; USD 110.000 - 170.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life insurance

Flexible benefits

Descripción de la vacante

ICON Strategic Solutions is seeking a Clinical Scientist – Oncology for a home-based role in the United States or Canada. You will support clinical studies through medical monitoring, data reconciliation, and materials preparation, interacting with study sites and committees to advance objectives.

The role emphasizes collaboration within a sponsor-dedicated model, with flexibility to travel up to 15% and eligibility to work in the US or Canada without visa sponsorship.

Formación

• 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

Responsabilidades

• 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

Conocimientos

Medical monitoring

Oral & written communication

Excel

PowerPoint

ePRO

Travel readiness

Educación

BS/BA/MS/PhD in Life Sciences

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

Herramientas

ePRO

Descripción del empleo

ICON Strategic Solutions is seeking a Clinical Scientist – Oncology for a home-based role in the United States or Canada. You will support clinical studies through medical monitoring, data reconciliation, and materials preparation, interacting with study sites and committees to advance objectives.

The role emphasizes collaboration within a sponsor-dedicated model, with flexibility to travel up to 15% and eligibility to work in the US or Canada without visa sponsorship.