Role OverviewAs 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. You will work closely with your team and stakeholders to deliver clinical research work to a high standard.
What You Will Do
Key responsibilities include completing and maintaining study regulatory binder and documents, hosting/facilitating oversight check-in visits, and ensuring that all demographic information is accurately recorded on the Case Report Form (CRF).
Why It Might Be a Fit
You will bring relevant clinical research experience, along with a Bachelor's degree in a relevant scientific discipline, and knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
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
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
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