Clinical Research Coordinator — Drive Trials & Patient Impact

ICON; Mississippi; On-site; USD 52,000 - 72,000; Full time

Job summary

ICON is seeking a Clinical Research Coordinator in McComb, MS to support sponsor-dedicated studies. You will design and analyze trials, interpret complex data, and contribute to advancing therapies that benefit patients worldwide.

You will coordinate studies, recruit and follow-up with participants, ensure regulatory compliance, manage trial data and documentation, and support study teams across the project lifecycle.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Experience in clinical research or healthcare settings preferred.
• Knowledge of FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
• Strong organizational, communication, and interpersonal skills; ability to work effectively in a team.
• Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.

Responsibilities

• Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
• Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
• Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
• Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
• Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.

Skills

Organizational skills

Communication skills

Interpersonal skills

Detail-oriented

Multitasking

Education

Bachelor's degree in a relevant scientific discipline

Job description

ICON is seeking a Clinical Research Coordinator in McComb, MS to support sponsor-dedicated studies. You will design and analyze trials, interpret complex data, and contribute to advancing therapies that benefit patients worldwide.

You will coordinate studies, recruit and follow-up with participants, ensure regulatory compliance, manage trial data and documentation, and support study teams across the project lifecycle.