Providing high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients.
Collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.
Serving as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.
Ensuring compliance with quality processes and requirements for assigned documents; assisting in determining best practices, methods and techniques for achieving optimal results.
Assisting with developing timelines, budgets, forecasts for assigned deliverables.
Representing the department at project launch meetings, review meetings, and project team meetings.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.