Position: Clinical Data Manager Our firm seeks a competent and professional Clinical Data Manager for a critical role in a high-performance environment. This is an excellent opportunity for professionals who value structured career advancement and meaningful impact. Primary Duties and Responsibilities: Develop SOPs, work instructions, and training materials for clinical operations teams. Develop SAS programs for SDTM/ADaM dataset creation and table, figure, listing generation. Review source data and ensure completeness, accuracy, and regulatory compliance. Provide clinical site training on data collection standards and regulatory requirements. Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Plan, monitor, and close clinical trials in compliance with GCP and ICH guidelines. Maintain trial master files and ensure ongoing audit-readiness and regulatory compliance. Monitor safety signals and liaise with pharmacovigilance teams for adverse event management. Required Qualifications: Commitment to ongoing professional learning and industry knowledge enhancement. At least 24 years of hands-on experience in a comparable professional setting. Bachelor's degree in a relevant discipline; master's degree or professional certification is preferred. Detail-oriented mindset with the ability to synthesise and present complex information clearly. Proficiency in relevant software and digital tools specific to the functional area. Ability to work both independently and in a team-oriented, collaborative environment. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. We look forward to welcoming a driven professional who shares our commitment to excellence and sustained impact.