Regulatory Affairs Consultant II — FDA Submissions Lead
Remotedxb
Syner-G, a biopharma product development partner, is seeking a regulatory affairs professional to oversee preparation, review and submission of regulatory documents. You will handle FDA meetings and author IND, NDA and BLA submissions, coordinating with clinical teams.
You will mentor junior staff and manage global regulatory communications with FDA and other authorities, supporting clients through development and submission processes.
#J-18808-LjbffrVacancy posted 22 hours ago
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