Clinical Study Coordinator

ICON plc • Washington, DC

1d

About The Position

Clinical Study Coordinator ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to این patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Clinical Study Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Requirements

• Bachelor's degree in a relevant scientific discipline.
• Proven experience as a Clinical Study Coordinator or in a similar role.
• Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Strong organizational and multitasking skills.
• Excellent communication and interpersonal abilities.
• Having the legal right to work in the country where the role is based.

Responsibilities

• Collaborating with cross-functional teams to develop and implement clinical trial protocols.
• Coordinating and overseeing the execution of clinical studies, ensuring adherence to protocols and regulatory requirements.
• Managing study timelines, budgets, and resources effectively.
• Facilitating communication between investigative sites, sponsors, and internal teams.
• Ensuring data accuracy and completeness through regular monitoring and quality control activities.

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

What This Job Offers

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