Review and draft CTD/eCTD dossier sections for UK MHRA submissions.
Prepare, review, and coordinate responses to UK MHRA Requests for Information (RFI) within defined timelines.
Ensure all dossiers comply with UK MHRA guidelines
📌 Clinical Data Associate (Mumbai)
🏢 Flamingo Pharmaceuticals
📍 Mumbai
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.