Senior Medical Information Writer
Core
Develop, review, and maintain scientifically accurate, evidence-based Medical Information (MI) content including Scientific Response Documents (SRDs), Global Response Documents (GRDs), FAQs, and training materials for biopharma and research clients.
Role type
Senior Medical Information Writer (Scientific Content & Compliance)
Builds
Scientific response documents, FAQs, training materials, and MI content for pharmaceutical, biotechnology, and medical device clients.
Domain
Life Sciences / Biopharma / Medical Information
Deliverable
client delivery
Required skills
Scientific writing, evidence synthesis, literature search, document lifecycle management, quality control, regulatory compliance knowledge, project management, reference management, Microsoft Office proficiency
Preferred skills
PharmD, PhD, or MD; Master's in scientific discipline; Veeva Vault Systems expertise; broad therapeutic area experience; advanced editing skills
Technologies
Veeva Vault Systems, PubMed, Ovid, Embase, EndNote, Mendeley, Citavi, Microsoft Office, Acrobat
Responsibilities
Develop and maintain MI content (SRDs, GRDs, FAQs); manage end-to-end content lifecycle including literature searches and MLR review coordination; conduct quality control and peer reviews; manage translation requests; support SOP and style guide development; participate in client-facing meetings; flag and manage quality issues.
Seniority
Senior, hands-on IC
