Position: TKI TA Head Oncology Global Pharmacovigilance We are seeking a highly qualified and motivated TKI TA Head Oncology Global Pharmacovigilance to join our dynamic and growing team. The selected professional will thrive in a data-driven, efficiency-focused, and collaborative work environment. Key Responsibilities: Conduct structured literature reviews and contribute to scientific summaries and labelling. Contribute to risk management plans, SOPs, and signal detection and evaluation processes. Coordinate with CROs and licensing partners to fulfil pharmacovigilance obligations. Support collection and review of adverse event safety data from clinical and post-market sources. Prepare high-quality clinical and regulatory documents aligned to CTD submission standards. Ensure audit-readiness of safety documentation in line with GxP and regulatory expectations. Ensure all cases are coded and processed per MedDRA and applicable global standards. Maintain up-to-date knowledge of ICH E2A-E2F, GCP, and pharmacovigilance regulations. Qualifications and Requirements: Proven ability to manage competing priorities in a deadline-driven, dynamic environment. High degree of professionalism, integrity, and alignment with organisational values. A bachelor's degree or higher in a relevant field; postgraduate qualifications are an added advantage. Experience collaborating within cross-functional teams and matrix organisational structures. Minimum 35 years of progressive professional experience in a comparable role. Strong analytical and problem-solving skills with the ability to navigate complex challenges. Knowledge of ICH E2A-E2F, MedDRA coding, GCP, and global regulatory requirements. We are committed to fostering an inclusive workplace and welcome applications from candidates of all backgrounds.