Onsite Clinical Trial Coordinator – 5-Month Contract

ICON Strategic Solutions; McComb (MS); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Competitive base salary and incentives

Health and wellbeing programs

Retirement and pension plans

Life assurance and disability coverage

Learning and development opportunities

Job summary

ICON Strategic Solutions is seeking a Clinical Research Coordinator for a 5-month, onsite contract in McComb, MS. You will design and analyze clinical trials, interpret complex medical data, and contribute to advancing innovative treatments.

Your role involves coordinating studies, recruiting participants, ensuring regulatory compliance, managing data, and supporting participants with procedures. A bachelor’s degree in a relevant field and experience in clinical research are preferred.

Qualifications

• Bachelor’s degree in a relevant scientific field or healthcare-related area.
• Experience in clinical research or healthcare settings preferred.
• Familiarity with FDA/EMA, ICH-GCP and HIPAA regulations.

Responsibilities

• Coordinate and execute clinical studies, including recruitment and follow-up.
• Collaborate with investigators, sponsors, and regulators to ensure compliance.
• Collect and maintain accurate trial data, including adverse events and outcomes.
• Manage study documentation and regulatory submissions.
• Provide participant support, education, and assistance with procedures.

Skills

Organizational skills

Communication

Interpersonal skills

Detail-oriented

Team collaboration

Education

Bachelor's degree in a relevant scientific field

Job description

ICON Strategic Solutions is seeking a Clinical Research Coordinator for a 5-month, onsite contract in McComb, MS. You will design and analyze clinical trials, interpret complex medical data, and contribute to advancing innovative treatments.

Your role involves coordinating studies, recruiting participants, ensuring regulatory compliance, managing data, and supporting participants with procedures. A bachelor’s degree in a relevant field and experience in clinical research are preferred.