PV Data Associate
London, England, United Kingdom
EPM Scientific
standards and company SOPs. Process cases and perform MedDRA coding of safety events as per the latest version. Enter and maintain data in the Pharmacovigilance Database. Monitor adverse events received via EEDR. Generate safety data for signal detection and periodic aggregate reports. Supply safety data to the regulatory department for … regulatory submissions. Contribute to the continuous enhancement of the pharmacovigilance system. Report ICSR and SUSAR via EVWEB post-training. Conduct medical and scientific literature searches. Skills and Competencies: Exceptional attention to detail. Proficient in computer use. Capable of planning, organizing, and following up. Ability to manage clinical activities to meet … agreed timelines. Stay updated with pharmacovigilance requirements. Effective communication skills in both individual and group settings. Ability to build and maintain relationships with internal and external stakeholders. Team player. Problem-solving abilities. Efficient time management skills across multiple tasks. Curious and inquisitive mindset. Qualifications and Experience: Desirable Qualifications: Degree in more »
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