Clinical Trial Associate: Trial Coordination & Compliance

ICON Clinical Research; United States; Remote; USD 48,000 - 68,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

Life assurance

Global EAP

Job summary

ICON Strategic Solutions seeks a Clinical Trial Associate to support clinical research activities within ICON's sponsor-dedicated model. You will assist in trial design and analysis, interpret medical data, and contribute to the advancement of treatments benefiting patients worldwide.

You will coordinate trial activities, maintain essential documents, and collaborate with cross-functional teams to ensure timely execution and accurate reporting of trial milestones.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Willingness to travel approximately 10%.

Responsibilities

• Assist in coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files and regulatory submissions.
• Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to tracking and reporting of clinical trial metrics and milestones.

Skills

Organizational skills

Communication skills

Team collaboration

Attention to detail

Willingness to travel

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions seeks a Clinical Trial Associate to support clinical research activities within ICON's sponsor-dedicated model. You will assist in trial design and analysis, interpret medical data, and contribute to the advancement of treatments benefiting patients worldwide.

You will coordinate trial activities, maintain essential documents, and collaborate with cross-functional teams to ensure timely execution and accurate reporting of trial milestones.