Nonclinical Editor Jobs

Contract Nonclinical Editor

Remote

30 hours per week

Summary

The nonclinical editor is responsible for performing quality reviews and editing of nonclinical documents, regulatory submissions, and other related documents.

Responsibilities

§ Reviews documents to ensure the integrity of the data presented.

§ Performs quality control checks of documents against source materials.

§ Checks for consistency according to current regulatory standards and guidelines.

§ Performs editorial reviews of documents for grammar, style, format, and internal writing conventions.

§ Verifies scientific logic and clarity of the document.

§ Assists other team members with supportive tasks related to document management, literature searches, reference management ˗ as requested.

Qualifications

§ Bachelor’s degree in science or biomedical sciences or journalism/English/communications.

§ 5+ years of relevant editing-related experience in the pharmaceutical industry.

§ Computer skills and expertise in relevant applications (eg, MS Office and Adobe Acrobat)

§ Expertise with AMA Manual of Style.

§ Experience with nonclinical and regulatory documents, ICH guidelines, and requirements of the FDA and other international regulatory agencies.

§ Excellent communication and organizational skills.

§ Detail oriented.

§ Ability to handle multiple tasks and deadlines.

§ Ability to prioritize efficiently.