Location
- Global
Category
The role
You'll focus on pharmacology as a principal-level medical writer, bringing extensive experience with m2.7.2 (Summary of Clinical Pharmacology Studies). You'll work with a team of lead and contributing writers to deliver high-quality clinical and regulatory documents for pharmaceutical and biotech clients. This is a contract, remote role. If this fits your expertise, reach out directly to Anna Perez McElhenny.
At a glance
- Level
- Senior
Tools and skills
Skills
Regulatory WritingMedical WritingBriefing MaterialsRegulatory SubmissionsInvestigator BrochuresClinical Study ReportsClinical Study ProtocolsPharmacology