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Clinical Research Coordinator- Associate- Office Based
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 Associate at ICON, you will support clinical research activities to ensure high-quality data, protocol adherence, and patient safety.
What You Will Do
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Supporting the setup, coordination, and day-to-day conduct of clinical studies in accordance with protocols, ICH-GCP, and applicable regulations.
- Assisting with patient screening, informed consent documentation, and enrolment activities under the supervision of site staff.
- Ensuring accurate and timely completion of source documents and electronic case report forms (eCRFs).
- Organising and maintaining study files, essential documents, and Trial Master File (TMF) content to support audit-readiness.
- Coordinating study visits, scheduling patient appointments, and ensuring required assessments and procedures are completed as per protocol.
- Collaborating with monitors, investigators, and internal teams to resolve data queries and support continuous quality improvement.
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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, nursing, pharmacy, or a related discipline, or equivalent experience in a clinical or healthcare setting.
- Initial experience in clinical research or a similar regulated environment is preferred.
- Basic understanding of clinical trial processes, GCP guidelines, and regulatory requirements, with a strong willingness to learn.
- Strong organisational skills with the ability to manage multiple tasks, priorities, and deadlines with accuracy.
- High level of attention to detail and commitment to data quality and patient safety.
- Effective communication and interpersonal skills, with the ability to work collaboratively with site staff and cross-functional teams.
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Employment with ICON
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
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.
Are you a current ICON Employee? Please click here to apply
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