Associate Medical Writer
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Job Location:
Monthly Salary:
Posted on:
7 hours ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Join Us as Associate Medical Writer Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years.
As part of our expert team youll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As Associate Medical Writer you will assist with the preparation of high-quality medical and scientific writing from planning and coordination through the delivery of final drafts to internal and external clients. You will collaborate with internal and external clients supporting and enabling effective and efficient communication that results in operational excellence.
What Youll Do:
Assists with researching writing and editing routine documents including clinical study reports and study protocols and summarizes data from clinical studies.
May assist with more complex clinical and scientific and program level documents including IBs INDs and MAAs.
Assists with ensuring compliance with quality processes and requirements for assigned documents.
May assist in program management activities. Duties could include assisting with developing timelines budgets and forecasts.
Participates in project launch meetings review meetings and project team meetings.
Education and Experience Requirements:
Bachelors degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 0 to 2 years).
Experience working in the pharmaceutical/CRO industry advantageous
Experience in scientific writing advantageous
In some cases an equivalency consisting of a combination of appropriate education training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role.
Knowledge Skills and Abilities:
Basic medical writing skills including grammatical editorial and proofreading skills
Ability to interpret and present complex data accurately and concisely
Effective administrative organizational and planning skills; attention to detail and quality
Ability to work on own initiative and effectively within a team
Effective oral and written communication skills
Basic knowledge of regulatory documentation and drug development process
Good judgment and decision-making
Competent computer skills and use of templates; basic knowledge of document management systems and other relevant applications (e.g. Excel Outlook)
Working Conditions and Environment:
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international.
Long varied hours required occasionally
Why Join Us
When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.
Apply today to help us deliver tomorrows breakthroughs.
Required Experience:
IC
Key Skills
- Clinical Research
- Adobe Acrobat
- FDA Regulations
- Technical Writing
- Biotechnology
- Clinical Development
- Clinical Trials
- Microsoft Powerpoint
- Research Experience
- Document Management Systems
- Word Processing
- Writing Skills
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
