Onsite Clinical Research Coordinator (5-Month Contract)

ICON Strategic Solutions; McComb (MS); On-site; USD 45,000 - 65,000; Full time

Job summary

ICON, a global healthcare intelligence and clinical research organization, is seeking a Clinical Research Coordinator for a 5-month onsite contract in McComb, MS. You will design and analyze trials, interpret medical data, and support the advancement of innovative treatments.

The role involves coordinating studies, ensuring regulatory compliance, managing data and docs, and assisting participants. Requires a Bachelor's in a relevant field and experience in clinical research.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Previous experience working in clinical research or healthcare settings preferred.
• Knowledge of FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
• Strong organizational, communication, and interpersonal skills.

Responsibilities

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

Skills

Clinical coordination

Regulatory compliance

Data management

Communication skills

Detail oriented

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Job description

ICON, a global healthcare intelligence and clinical research organization, is seeking a Clinical Research Coordinator for a 5-month onsite contract in McComb, MS. You will design and analyze trials, interpret medical data, and support the advancement of innovative treatments.

The role involves coordinating studies, ensuring regulatory compliance, managing data and docs, and assisting participants. Requires a Bachelor's in a relevant field and experience in clinical research.