CRC Level 1

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to 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. This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

As a CRC Level 1 at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

• You will take responsibility for clinical coordination deliverables, applying your skills to ensure quality and efficiency.
• Key responsibilities include:
• Assisting in the coordination and implementation of clinical trial activities under the guidance of Clinical Research Coordinators (CRCs), including patient recruitment, screening, and enrollment.
• Supporting the maintenance and organization of study documentation and regulatory files, ensuring compliance with protocol requirements and regulatory standards.
• Collecting, recording, and entering data into study databases and electronic data capture (EDC) systems, in accordance with study protocols and standard operating procedures (SOPs).
• Assisting with the preparation and submission of regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs).
• Providing logistical support for study visits, meetings, and other research-related activities, including scheduling appointments, arranging travel, and coordinating study materials.

Your Profile:

You will bring relevant clinical coordination experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in life sciences, healthcare, or related field; relevant experience may be considered in lieu of a degree.
• Previous experience in clinical research or healthcare setting is preferred but not required.
• Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities effectively.
• Excellent communication and interpersonal skills, with the ability to interact professionally with study participants and colleagues.
• Proficiency in Microsoft Office suite (Word, Excel, Outlook) and willingness to learn new software applications as needed.

Rewards & Benefits:

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:

• 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

Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility:

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.