The contractor shall have a scientific background to work directly with nonclinical study teams, research scientist, project managers and Regulatory affairs personnel to prepare complex report documents from raw
and/or processed data. Specific tasks include:
* Prepare documents to include but are not limited to: Protocols and protocols amendments, research and nonclinical study reports, and FDA animal rule submission document in compliance with FDA/GLP regulations Shall manipulate data and scientific findings in appropriate table and text for presentation in logical fashion. Documents review totaling 3-6 per month.
* Will attend meeting and participate in study and project meetings to provide input regarding deliverable, timelines and processes as needed. Attends 2-4 meetings per month.
Bachelors Degree in English, Journalism or a related discipline.
5-8 years of related experience preparing and editing technical documentation.
As a trusted systems integrator for more than 50 years, General Dynamics Information Technology provides information technology (IT), systems engineering, professional services and simulation and training to customers in the defense, federal civilian government, health, homeland security, intelligence, state and local government and commercial sectors.With approximately 32,000 professionals worldwide, the company delivers IT enterprise solutions, manages large-scale, mission-critical IT programs and provides mission support services.GDIT is an Equal Opportunity/Affirmative Action Employer - Minorities/Females/Protected Veterans/Individuals with Disabilities.
Department: Technical Operations (TechOps)