Remote Clinical Trial Associate | Home-Based (CDMX)

ICON Clinical Research; United States; Remote; USD 60,000 - 85,000; Full time

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Associate to work in a sponsor-dedicated model, supporting the design and analysis of clinical trials and interpreting complex medical data to advance treatments that benefit patients worldwide.

Your role involves coordinating trials, maintaining study documentation, preparing informed consent and case report forms, and collaborating with cross-functional teams to ensure smooth trial execution and timely milestones.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field is required.
• 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 the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files, essential documents, 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 the tracking and reporting of clinical trial metrics and milestones.

Skills

Clinical research interest

Organization

Communication skills

Team collaboration

Detail-oriented

Travel willingness

Education

Bachelor's degree in sciences/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Trial Associate to work in a sponsor-dedicated model, supporting the design and analysis of clinical trials and interpreting complex medical data to advance treatments that benefit patients worldwide.

Your role involves coordinating trials, maintaining study documentation, preparing informed consent and case report forms, and collaborating with cross-functional teams to ensure smooth trial execution and timely milestones.