Clinical Trial Educator

Icon • Blue Bell, PA

2d

About The Position

Clinical Study Manager 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 Trial Liaison to join our diverse and dynamic team. Working as a Clinical Trial Educator, exclusively assigned and embedded within a Pharmaceutical Company, you will play a critical role in supporting clinical trial sites by delivering comprehensive education and training. What you will be doing This position ensures that investigators, coordinators, and healthcare professionals fully understand study protocols, eligibility criteria, and operational procedures. The primary objective is to enhance site readiness and protocol compliance through tailored educational programs and in-service presentations. The Clinical Trial Educator (CTE) collaborates closely with Contract Research Organizations (CROs) and field-based medical teams to address knowledge gaps and provide ongoing educational support. Responsibilities include training site staff in medical or nursing procedures, clarifying study requirements, facilitating understanding of therapeutic areas, and ensuring adherence to Good Clinical Practice (GCP) standards. This is a field-based position that may require extensive domestic or international travel, depending on project needs

Requirements

• Bachelor's degree in a relevant field, such as life sciences or healthcare.
• Experience in clinical trial education and clinical research.
• Clinical experience in Neurology and/or Immunology.
• Fluency in English.
• Excellent written and verbal communication skills.
• Strong in-person and virtual presentation skills.
• Active license or credential in one of the following: MD (Medical Doctor), RN (Registered Nurse), DO (Doctor of Osteopathic Medicine), NP (Nurse Practitioner), Pharmacist (RPh or PharmD).
• Willingness and ability to travel domestically and/or internationally up to 75%.
• Proficiency with Microsoft Office applications.

Nice To Haves

• Certified Clinical Research Coordinator (CCRC).
• 2+ years of experience providing site training in healthcare.
• RN/Nurse with infusion nursing experience.
• Experience in protocol training and site engagement.

Responsibilities

• Training site staff in medical or nursing procedures
• Clarifying study requirements
• Facilitating understanding of therapeutic areas
• Ensuring adherence to Good Clinical Practice (GCP) standards

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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees