• Play an active role in planning, conduct and evaluation of ongoing clinical trials to ensure successful execution • Support medical monitoring activities for ongoing clinical trials. • Support/manage preparation of materials for trial-related clinical committees such as Data Monitoring Committees, Adjucation Committees, etc. • Contribute to planning, authoring, and critical review of documents submitted to regulatory authorities and ethics committee/IRBs as required (e.g., Protocols, CSRs, IB, clinical briefing documents). • Contribute to the strategic planning, authoring, and critical review of scientific data disclosures (e.g., slide presentations, posters and publications). • Co-ordinate aggregate report preparation (e.g., DSURs, PSUSARs, ASR), and safety management plans (SMPs) in collaboration with external vendors • Contribute to engagement with external stakeholders such as vendors, thought leaders or other groups as needed including being the primary liaison with assigned individuals or groups. • Function as an independent member of the team and represent clinical research at internal cross-functional or external meetings. • Other duties related to clinical development of EFX as assigned.