Home based - CDMXICON plc is a world-leading healthcare intelligence and clinical research organization.
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
What You Will Do
You will take ownership of pharmacovigilance and drug safety deliverables, applying your expertise to complex challenges.
Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies.
Conducting thorough data analysis and interpretation of safety data, identifying trends and potential safety signals that require further investigation.
Preparing and submitting comprehensive periodic safety update reports (PSURs) and other regulatory documents, ensuring compliance with international regulations.
Collaborating with medical and clinical teams to assess the...