Remote Medical Writer - Clinical Trials Documentation
Lotus Clinical Research, LLC
New York, NY
- Remote job
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-Ljbffr Lotus Clinical Research, LLC
Vacancy posted 2 days ago
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