Clinical Data Coordinator

• Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures
• Review clinical and third-party data based on edit specifications and data review plans
• Issue clear, accurate, and concise queries to investigational sites
• Communicate effectively with peers, clinical data scientist and functional management
• Perform project activities such as filing and archiving study documentation and dispatching queries to investigator sites for resolution
• Ensure study timelines are met

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare
• Basic knowledge of 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
• 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