A global staffing and IT consulting company is seeking a Medical Writer to coordinate and author documents for regulatory submissions. The ideal candidate should have a PhD/MD/PharmD in a relevant scientific discipline or equivalent experience in pharmaceutical regulatory documentation. Strong writing skills, organizational abilities, and experience working in cross-functional teams are essential. This role involves participating in document strategy sessions and ensuring high-quality deliverables within set timelines.
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Medical Writer: Regulatory Submissions & CSRs in pennington at Unknown Company
This position is listed as full time and onsite.