Remote Clinical Scientist, Oncology & Specialty Trials

ICON; Little Canada (MN); Remote; USD 90,000 - 130,000; Full time

Job summary

ICON is seeking a Clinical Scientist to support oncology and specialty studies in a sponsor-dedicated model. The role includes clinical conduct of trials, protocol management, medical monitoring, and stakeholder coordination, with remote work in the US or Canada.

The candidate will collaborate with study teams, sites, and external committees, handling imaging data reconciliation and meeting materials, and may lead limited-scope studies such as survival follow-ups.

Qualifications

• BS/BA/MS/PhD in Life Sciences with 2+ years relevant experience, or 5+ years clinical development experience without life sciences degree.
• Experience in Oncology, Infectious Disease/Vaccines, Neurology, Cardiology, or Immunology.
• Medical monitoring experience (2+ years highly preferred).
• Proficiency in Excel and PowerPoint; ePro experience a plus.
• Strong oral and written communication skills.
• Legal authorization to work in US and/or Canada; no visa sponsorship required.
• Willingness to travel up to 15% including potential international travel.

Responsibilities

• Support clinical and scientific conduct of studies including adjudication, medical monitoring, and protocol deviation management.
• Prepare imaging data reconciliation and meeting materials for study teams and stakeholders.
• Support single or multiple studies; may lead limited-scope studies such as survival follow-ups.
• Collaborate with internal teams, study sites, and external committees to advance clinical study objectives.

Skills

Medical monitoring

Clinical trial coordination

Communication skills

Excel

PowerPoint

ePro experience

Travel readiness

Education

BS/BA/MS/PhD in Life Sciences

Tools

Excel

PowerPoint

Job description

ICON is seeking a Clinical Scientist to support oncology and specialty studies in a sponsor-dedicated model. The role includes clinical conduct of trials, protocol management, medical monitoring, and stakeholder coordination, with remote work in the US or Canada.

The candidate will collaborate with study teams, sites, and external committees, handling imaging data reconciliation and meeting materials, and may lead limited-scope studies such as survival follow-ups.