About this opportunity
ICON Clinical Research lists this Senior Medical Writing Lead: Regulatory & Study Docs opportunity in center square, Pennsylvania. Review the employer’s description below for duties, qualifications and application requirements.
Job description
ICON Clinical Research in Center Square, PA is seeking a senior Medical Writing Manager to coordinate delivery of medical writing projects, resolve issues, and build team capability. You will lead the medical writing team to ensure high-quality, scientifically sound documentation across regulatory submissions, CSRs, protocols, and investigator brochures.
You will collaborate with clinical, regulatory, and project management teams to maintain regulatory compliance, align timelines, and
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.