Senior Pharmacovigilance Officer

b Overview /b p In this role you will oversee safety reporting activities within the CTC to protect patient safety and ensure regulatory compliance. You will work with the Regulatory team to manage SUSAR reviews, queries, and timely submissions to ICSR and EudraVigilance, and you will oversee DSUR submissions to MHRA. This position sits at the intersection of pharmacovigilance and clinical trial operations in an academic sponsor setting. You will collaborate with trial teams to maintain high-quality safety data and support ongoing cancer research initiatives. This is a full-time, open-ended role with hybrid work options and a focus on managing risk and regulatory reporting at scale. /p b Pay / Benefits /b ul li 41 days holiday /li li pension CARE /li li cycle to work /li li on-site nursery /li li on-site gym /li li relocation scheme /li /ul b Responsibilities /b ul li review SUSAR reports and raise queries with trial teams /li li submit and maintain SUSAR submissions in ICSR and EudraVigilance portals /li li ensure timely DSUR submissions to MHRA /li li maintain oversight of safety reporting activities and ensure ongoing regulatory compliance /li li collaborate with trial teams to resolve safety-related issues /li /ul b Key requirements /b ul li significant knowledge of biomedical or life sciences /li li significant experience in pharmacovigilance within an academic sponsor setting /li li experience in safety reporting to competent authorities and REC /li li proficient with ICSR Submissions and EudraVigilance /li li experience in preparing DSURs /li li knowledge of cancer biology and treatments (advantageous) /li /ul ul li pharmacovigilance /li li SUSAR reporting /li li ICR Submissions /li li EudraVigilance /li li DSUR preparation /li li MHRA regulatory submissions /li /ul