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ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
Senior Clinical Data Coordinator, Standards
Senior coordinator overseeing clinical trial data and standards for ICON’s sponsor-dedicated research programs. Supports data quality, compliance, reconciliation, and timely study delivery.
Description
- Plan and assess clinical trials, interpret complex medical data, and support the development of new treatments and therapies.
- Lead technically demanding clinical research activities, prioritizing quality and ongoing improvement.
- Develop and maintain data management plans and study records in line with industry standards and regulatory requirements.
- Find and resolve data inconsistencies to improve data flow and quality across the study lifecycle.
- Work with clinical operations and biostatistics teams to design and carry out study-specific data management approaches.
- Complete project work to keep studies on schedule, including filing and archiving records and sending queries to investigator sites.
- Guide junior data coordinators in data reconciliation, coding, and cleaning practices.
Requirements
- Bachelor’s degree in a relevant discipline, such as life sciences or healthcare.
- Demonstrated clinical data management experience in the pharmaceutical or biotechnology industry.
- Familiarity with clinical data management tools such as Medidata, Oracle RDC, or similar systems.
- Strong attention to detail and effectiveness in a fast-paced work environment.
- Excellent communication and ability to work with cross-functional teams.
- Knowledge of regulatory guidance and standards, such as ICH-GCP, is an advantage.
- Willingness to travel as needed, approximately 5%.
- Must have legal authorization to work in the country where the role is based; employment with ICON is conditional on this.
Benefits
- Competitive base pay and performance-based incentives.
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life insurance and disability coverage.
- Employee assistance programs and wellbeing resources.
- Learning and development through structured training and career pathways.
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