Position: Bioinformatics Analyst We are currently recruiting a results-oriented Bioinformatics Analyst to strengthen our high-performing team. This is an excellent opportunity for professionals who value structured career advancement and meaningful impact. Primary Duties and Responsibilities: Prepare and maintain essential trial documents including protocols, ICFs, and CSRs. Conduct benefit-risk assessments and contribute to clinical development strategy discussions. Maintain trial master files and ensure ongoing audit-readiness and regulatory compliance. Develop SOPs, work instructions, and training materials for clinical operations teams. Track milestones and coordinate with sites, CROs, and sponsors for on-time delivery. Review source data and ensure completeness, accuracy, and regulatory compliance. Monitor safety signals and liaise with pharmacovigilance teams for adverse event management. Manage medical coding using MedDRA and WHO Drug Dictionary for clinical trial data. Required Qualifications: Bachelor's degree in a relevant discipline; master's degree or professional certification is preferred. Proficiency in relevant software and digital tools specific to the functional area. Exceptional organisational skills with the ability to handle multiple concurrent responsibilities. At least 24 years of hands-on experience in a comparable professional setting. Strong interpersonal and stakeholder management skills with a client-service orientation. Commitment to ongoing professional learning and industry knowledge enhancement. 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.