Clinical Trial Assistant - Early Development - Home Based

ICON Strategic Solutions; United States; Remote; USD 50,000 - 70,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Assistant for their Early Development team, offering a home-based position. This critical role involves managing trial logistics, ensuring regulatory compliance, and supporting site activities. Applicants should hold a relevant degree and have 1-2 years of clinical trial experience. ICON promotes an inclusive culture and provides competitive offerings focused on well-being, benefits, and professional growth.

Benefits

Annual leave

Health insurance

Retirement plans

Global Employee Assistance Program

Life assurance

Flexible benefits

Qualifications

• 1-2 years of relevant clinical trial experience.
• Legally authorized to work in the US without sponsorship.

Responsibilities

• Ensure trial activities comply with regulations and SOPs.
• Manage documents and logistical tasks for trial activities.
• Coordinate with sites and internal teams for trial materials.

Skills

Organizational skills

Interpersonal skills

Negotiation skills

Proficiency in English

MS Office

Education

BA/BS in Life Sciences, Nursing, or related field

Tools

VeevaVault TMF

Job description

Clinical Trial Assistant - Early Development - Home Based

Join to apply for the Clinical Trial Assistant - Early Development - Home Based role at ICON Strategic Solutions.

As a Clinical Trial Assistant, you will join the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence.

What You Will Be Doing

Ensure trial activities comply with GCO SOPs, policies, GCP, HCC, and local regulations. Responsibilities include reviewing regulatory documents, managing site activities, and supporting trial logistics.

• Manage documents and logistical tasks for trial start-up, execution, and close-out.
• Adhere to applicable SOPs, WIs, policies, and regulations.
• Maintain trial documentation and ensure audit readiness.
• Coordinate with sites and internal teams to ensure timely delivery of trial materials.
• Support budget management and training organization if applicable.

You Are

• BA/BS in Life Sciences, Nursing, or related field (or equivalent experience).
• 1-2 years of relevant clinical trial experience.
• Proficient in English and MS Office.
• Strong organizational, interpersonal, and negotiation skills.
• Experience with VeevaVault TMF is desirable.
• Legally authorized to work in the US without sponsorship.

Home Based US

What ICON Can Offer You

Competitive salary, benefits focused on well-being, and a diverse, inclusive culture.

• Annual leave, health insurance, retirement plans.
• Global Employee Assistance Program, life assurance, and flexible benefits.

Visit our benefits page for more info.

ICON is committed to diversity and inclusion. We provide accommodations for applicants with disabilities. Learn more at our accommodations page.

Additional Details

• Seniority level: Entry level
• Employment type: Full-time
• Job function: Research, Analysis, IT
• Industry: Pharmaceutical Manufacturing

This job is active and accepting applications.