Position: Clinical Data Manager Join our forward-thinking team as a Clinical Data Manager and play a pivotal role in our continued success. This position is embedded within a high-functioning team that prizes collaboration, innovation, and quality. Role Responsibilities: Provide clinical site training on data collection standards and regulatory requirements. Develop SOPs, work instructions, and training materials for clinical operations teams. Develop SAS programs for SDTM/ADaM dataset creation and table, figure, listing generation. Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Maintain trial master files and ensure ongoing audit-readiness and regulatory compliance. Track milestones and coordinate with sites, CROs, and sponsors for on-time delivery. Review source data and ensure completeness, accuracy, and regulatory compliance. Plan, monitor, and close clinical trials in compliance with GCP and ICH guidelines. Education and Experience Requirements: Excellent verbal and written communication skills; fluency in English is essential. Demonstrated proficiency with industry-standard tools, platforms, and methodologies. Experience collaborating within cross-functional teams and matrix organisational structures. A bachelor's degree or higher in a relevant field; postgraduate qualifications are an added advantage. Proven ability to manage competing priorities in a deadline-driven, dynamic environment. Minimum 35 years of progressive professional experience in a comparable role. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. Applications are reviewed on a rolling basis; suitably qualified individuals are encouraged to apply promptly.