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2017-44080

2017-44080

Title 
Director, Medical Writing
Job Locations 
-
US-Remote
Posted Date 
11/29/2017

More information about this job

Overview

Oversees deliverables, supervises employees, and provides expertise in the area of regulatory writing, publications writing, and regulatory publishing.

Responsibilities

•    Works with project teams to prepare clinical regulatory documents under strict timelines.
•    Trains and mentors other medical writers.
•    Ensures efficient publishing of documents.
•    Coordinates writing activities with the project teams for document development.
•    Provides strategic direction for regulatory writing, publication writing, or regulatory publishing programs

 

Qualifications

9 years of leadership experience in clinical and scientific communications, including 5 years of formal people management experience

Bachelor’s degree

Early Clinical and Nonclinical Experience preferred



PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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