ICON plc
ICON plc
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

Coordinate clinical trial data and study records for ICON’s sponsor-dedicated pharmaceutical research programs. Maintain data quality, regulatory compliance, and on-time study delivery.

Description

  • Plan and analyse clinical trials, interpreting complex medical data
  • Lead technically demanding clinical research tasks, promoting quality and ongoing improvement
  • Prepare and maintain data management plans and records in line with industry standards and regulatory requirements
  • Resolve data discrepancies and other issues to improve data flow and quality across the study lifecycle
  • Work with clinical operations, biostatistics, and other teams to shape and carry out study-specific data management strategies
  • File and archive study records and send queries to investigator sites as part of project work
  • Guide junior coordinators in data reconciliation, coding, and cleaning
  • Keep study activities on schedule

Requirements

  • Bachelor’s degree in a relevant discipline, such as life sciences or healthcare
  • Demonstrated clinical data management experience in the pharmaceutical or biotechnology sector
  • Familiarity with data management platforms such as Medidata, Oracle RDC, or comparable systems
  • Strong attention to detail and effectiveness in a fast-paced setting
  • Clear communication skills and ability to work across teams
  • Knowledge of regulatory guidance and standards such as ICH-GCP is an advantage
  • Availability to travel when needed, approximately 5%
  • Legal authorization to work in the country where the position is based

Benefits

  • Base salary with performance-related 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
  • Training and career development through structured learning opportunities

Related Jobs

Saga

Business Development Representative, Germany (Remote)

Saga

Help Saga grow its legal technology business in Germany by building qualified sales opportunities for its AI offering. The role combines prospect outreach, partner development, and representation at legal technology events.

Open