Clinical Scientist — Design, Analyze & Elevate Trials

ICON Strategic Solutions; United States; On-site; USD 100,000 - 150,000; Full time

Job summary

ICON Strategic Solutions seeks a Clinical Scientist to design and conduct clinical studies advancing understanding of new therapies. You will work in a sponsor-dedicated model, supported by ICON’s global expertise and a collaborative environment that prioritizes patient impact.

The role emphasizes responsible clinical research deliverables, data analysis, and cross-functional teamwork, with travel up to 20% as part of regulatory submissions and publications.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Experience in clinical research with understanding of trial processes.
• Strong analytical and data interpretation skills.
• Excellent communication and collaboration abilities.
• Willingness to travel ~20%.
• Detail-oriented with data integrity.

Responsibilities

• Design and implement clinical trial protocols, ensuring adherence to scientific and regulatory standards.
• Conduct data analysis and interpretation to derive insights that support study objectives.
• Collaborate with cross-functional teams to ensure study execution and data quality.
• Engage with stakeholders to communicate findings and contribute to scientific discussions.
• Assist in the preparation of regulatory submissions, study reports, and scientific publications.

Skills

Clinical research

Data analysis

Regulatory understanding

Statistical analysis

Communication

Team collaboration

Travel willingness

Education

Bachelor's degree in a relevant field

Job description

ICON Strategic Solutions seeks a Clinical Scientist to design and conduct clinical studies advancing understanding of new therapies. You will work in a sponsor-dedicated model, supported by ICON’s global expertise and a collaborative environment that prioritizes patient impact.

The role emphasizes responsible clinical research deliverables, data analysis, and cross-functional teamwork, with travel up to 20% as part of regulatory submissions and publications.