Kura Oncology is seeking a seasoned Director/Associate Director of Medical Writing to lead regulatory document strategy and execution. You will partner with clinical, regulatory and medical affairs teams to deliver CSRs, protocols, and briefing books on aggressive timelines.
You will manage vendors, SOPs, and templates while ensuring compliance with ICH and FDA guidelines. A senior, cross-functional role in a fast-paced biotech setting with generous benefits awaits.
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