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Job description
ProPharma is seeking a senior medical writing/quality control leader to drive departmental growth, improve processes, and lead cross-functional coordination in a hybrid setup. The role emphasizes client relationship management and strategic capability development within regulatory frameworks.
The ideal candidate has 7+ years in medical writing/QA for drugs, biologics, or devices, plus 5+ years in project/resource management, and a strong track record in business development and mentoring teams.
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Worksite address
raleigh, NC, 27601, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.