Lotus Clinical Research, LLC is seeking a Contract Medical Writer to support regulatory writing for clinical trials from a remote US-based position. The role involves authoring and editing protocols, investigator brochures, CDSR/IND submissions, and related documents with strict adherence to GCP/ICH guidelines.
The candidate will collaborate with cross-functional teams, develop templates, manage timelines, and ensure compliance with SOPs and quality standards across Phase I–IV studies; a BS/BA
#J-18808-LjbffrRemote Medical Writer – Clinical Trials Documentation in id at Unknown Company
This position is listed as contract and able to be worked remotely.