Associate Director, Regulatory Medical Writing, Oncology
Johnson & Johnson
High Wycombe, Buckinghamshire, United Kingdom
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Regulatory medical writing
Oncology therapeutic area
Lead complex documents
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Johnson & Johnson is seeking an Associate Director for Regulatory Medical Writing specializing in Oncology to lead and oversee the writing process for clinical and regulatory documents. The ideal candidate will have extensive experience in medical writing, project management, and people management, along with a commitment to innovation in healthcare.
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Job Summary
Lead in setting functional tactics and strategy, and represent the therapeutic area head at high-level meetings.
Responsible for writing and coordinating complex clinical and regulatory documents, establishing and driving document timelines and strategies independently.
Supervise and manage direct reports, setting objectives, providing performance oversight, and ensuring adherence to established policies.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking an Associate Director for Regulatory Medical Writing specializing in Oncology to lead and oversee the writing process for clinical and regulatory documents. The ideal candidate will have extensive experience in medical writing, project management, and people management, along with a commitment to innovation in healthcare.
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Skills & Requirements
Must-have
Regulatory Medical Writing
Oncology therapeutic area
Lead complex documents
People management experience
Process improvement leadership
Nice-to-have
Champion internal standards
Develop best practices
Act as change agent
Inclusive leadership
Internalize CREDO behaviors
Key Requirements
Bachelor's Degree required
10+ years pharmaceutical/scientific experience
8+ years clinical/regulatory medical writing experience