Senior Clinical Data Coordinator

• Design and analyse clinical trials, interpreting complex medical data
• Lead clinical research tasks requiring technical depth, with a focus on quality and continuous improvement
• Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements
• Identify and resolve data discrepancies and issues to streamline data flow and enhance data quality throughout the study lifecycle
• Collaborate with clinical operations, biostatistics, and other cross-functional teams to develop and execute study-specific data management strategies
• Perform project activities such as filing and archiving study documentation and dispatching queries to investigator sites
• Mentor junior data coordinators on data reconciliation, coding, and cleaning procedures
• Ensure study timelines are met

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare
• Proven experience in clinical data management within the pharmaceutical or biotechnology industry
• Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar)
• Strong attention to detail and the ability to work effectively in a fast-paced environment
• Excellent communication skills and the ability to collaborate with cross-functional teams
• Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus
• Willingness to travel as required (approximately 5%)
• Legal right to work in the country where the role is based

• 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