Clinical Study Coordinator

ICON plc • San Antonio, TX

5d • Onsite

About The Position

Clinical Research Coordinator- Early Phase Research-ICON San Antonio TX ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Coordinator to join our diverse and dynamic team. As a Clinical Research Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Title: Clinical Research Coordinator Job Type: Full Time/Permanent Location: 100% On-Site San Antonio TX

Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Previous experience working in clinical research or healthcare settings preferred.
• (Experience as a Clinical Research Coordinator 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.

Nice To Haves

• Experience as a Clinical Research Coordinator preferred

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.

Benefits

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level