Senior Regulatory Affairs CMC Lead - Global Submissions
Remotedxb
Iovance Biotherapeutics in Dubai, UAE seeks an experienced Regulatory Affairs professional to oversee CMC dossier preparation and submissions for clinical and commercial programs. You will align eCTD documentation with global requirements and maintain submission trackers while coordinating with vendors and CROs.
Ideal candidates have 8+ years in regulatory affairs, a strong science background, and proficiency with MS Office and Adobe Acrobat Pro.
#J-18808-LjbffrVacancy posted 1 day ago
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