Senior Clinical Research Coordinator
ICON plc
Summary
As a Senior CRC, you will coordinate and manage the operational aspects of clinical trials, including participant recruitment, scheduling, and site logistics, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards throughout the trial.
Job description
Key responsibilities include:
- Support day-to-day clinical trial activities, including pre-screening, recruitment, and participant-related study activities, as applicable
- Conduct the informed consent process and educate participants on study requirements and procedures
- Review inclusion/exclusion criteria and support patient screening and enrollment
- Perform timely and accurate clinical trial data entry within CTMS and EMR systems and resolve data queries in accordance with study requirements
- Collaborate with investigators, monitors, and study team members to support effective study conduct, including monitoring visits and investigator meetings
- Maintain accurate and complete study-related documentation and information in applicable study systems
- Communicate patient status, recruitment progress, study needs, and safety information to investigators and study leadership
- Support protocol-mandated study visits and procedures, as applicable, excluding investigational product dosing and unblinded IP accountability
- Partner with investigators and the study team to support regulatory requirements and overall study execution
Requirements
- 2+ years of experience as a Clinical Research Coordinator
- Experience with EPIC or another comparable EMR
- Experience with Medidata Rave or another CTMS
- Good understanding of clinical trial processes, GCP, and site documentation requirements
- Excellent time management and planning skills with an organized approach to work
- Bachelor's degree in life sciences, healthcare, or a related field
- Experience with Phase III and/or Cardiology trials (preferred)
Benefits
- Competitive base salary
- Performance related incentives
- Medical, Dental & Vision
- Retirement and pension plans
- Life assurance
- Disability coverage
- Employee assistance programmes
- Wellbeing resources
- Learning and development opportunities
Company overview
ICON plc is a global leader in clinical research and healthcare intelligence, founded in Dublin, Ireland in 1990. As one of the world's largest contract research organizations (CROs), ICON provides comprehensive outsourced development services to pharmaceutical, biotechnology, and medical device companies worldwide. The company operates in 55 countries with approximately 41,900 employees, offering end-to-end solutions that span the entire product development lifecycle. ICON's service portfolio includes clinical research services, adaptive trials, biosimilars, commercialization and outcomes consulting, medical imaging, laboratory services, and strategic support for traditional and digital health technologies. The company specializes in therapeutic areas such as oncology, cardiovascular diseases, central nervous system disorders, rare diseases, and women's health. With its 2021 acquisition of PRA Health Sciences, ICON significantly expanded its capabilities and market position, becoming a dominant force in the global CRO industry. The company is publicly traded on NASDAQ under the ticker ICLR and reported $8.28 billion in revenue for 2024.