CMC Regulatory Affairs Associate II: Global Submissions

Iovance Biotherapeutics is seeking a Regulatory Affairs professional to manage CMC dossier content submission for clinical and commercial applications. The role involves preparing global submission documents following eCTD specifications and maintaining trackers and logs for submissions and correspondence.

The candidate will support regulatory strategy from IND through NDA/BLA and commercialization, coordinating with vendors and CROs to ensure timely submissions and high-quality deliverables.