Clinical Research Coordinator

About the role

As a Clinical Research Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Responsibilities

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

Required qualifications and experience

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