Senior Medical Writer

Company Details

Piper Companies

Piper Companies is currently seeking Senior & Principal Medical Writers for a fully REMOTE opportunity to join a global clinical research organization.


Responsibilities of the Sr. / Principal Medical Writer:

  • Write, review, and QC for multiple study related regulatory documents including protocols, clinical study reports (CSRs), manuscripts, informed consent forms (ICFs), and investigator brochures (IBs)
  • Interpret reports, data and statistical results from clinical trials in order to write and develop manuscripts, abstracts, study reports, presentations, and posters
  • Assist with editing, reviewing and QC of regulatory documents and submissions for clinical trials
  • Work with cross-functional teams to ensure IND and NDA submissions are completed on time

Qualifications of Sr. / Principal Medical Writer:

  • 4+ years of experience in medical writing role in a pharmaceutical company or CRO
  • 3+ years of electronics documents/submissions – required
  • Phase II & III experience – preferred
  • Therapeutic indications preferred – Oncology, GI, Infectious Disease, Immunology, or Vaccinations
  • PhD in a Scientific, Clinical, or Regulatory field – preferred

Compensation for the Sr. / Principal Medical Writer:

  • Pay commensurate with experience
  • Full Time-Permanent/or Contract
  • Comprehensive benefits package


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