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Veristat is seeking a Senior Medical Writer to independently plan and prepare regulatory documents for all phases of product development. You will organize, analyze, and present scientific information in line with ICH and company standards, while collaborating with cross‑functional teams on document production.
Ideal candidates have a minimum of 5 years in medical writing within CRO or pharma settings, with excellent English and strong attention to detail.
Senior Medical Writer
The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Senior Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.
Job Description
Senior Medical Writer
The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with International Council for Harmonisation (ICH) and other regulatory guidelines, and individual company document standards. The Senior Medical Writer works under the direction of Medical Writing management and collaborates with cross-functional internal and external document production teams.
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