Clinical Research Coordinator: Trials & Compliance Lead

ICON Strategic Solutions; Pennsylvania; On-site; USD 45,000 - 62,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life insurance

Flexible benefits

Job summary

ICON plc is seeking a Clinical Research Coordinator in McComb, MS to deliver high-standard clinical coordination work. You will collaborate with teammates and stakeholders to drive studies forward, ensure protocol compliance, and support participants throughout the trial.

The role emphasizes data integrity, regulatory knowledge, and strong communication within a dynamic team, with ICON offering comprehensive benefits and inclusive culture.

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.
• Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.

Responsibilities

• Facilitate coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
• Collaborate with principal investigators, sponsors, and regulatory authorities to ensure compliance with study protocols and regulatory requirements.
• Collect and maintain accurate clinical trial data, including adverse events, protocol deviations, and study outcomes.
• Manage study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
• Provide education, counseling, and assistance to study participants regarding procedures.

Job description

ICON plc is seeking a Clinical Research Coordinator in McComb, MS to deliver high-standard clinical coordination work. You will collaborate with teammates and stakeholders to drive studies forward, ensure protocol compliance, and support participants throughout the trial.

The role emphasizes data integrity, regulatory knowledge, and strong communication within a dynamic team, with ICON offering comprehensive benefits and inclusive culture.