A Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Information Technology, or a related field, OR equivalent work experience in drug safety management and/or signal evaluation.
Proven experience in business analysis, particularly within the pharmaceutical or life sciences sector.
Deep understanding of drug safety management, signal evaluation processes, and pharmacovigilance systems.
Basic familiarity with data science, and statistical modelling techniques used in clinical safety processes.
Familiarity with regulatory frameworks like FDA, EMA, and ICH guidelines.
Proficiency in tools such as JIRA, Confluence, Visio, and SQL is preferred.
Strong analytical, problem-solving, and communication skills.
Ability to work collaboratively with diverse teams in a fast-paced environment