Join Us as a Senior Medical Writer - Make an Impact at the Forefront of Innovation
The Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior Medical Writer may assist program manager. The role involves collaborating with internal and external clients supporting and enabling effective and efficient communication that results in operational excellence.
Key Responsibilities
- Drive the operational framework for CDO Medical Writing ensuring timely high-quality document delivery.
- Enable operational excellence through planning coordination project management and technical support.
- Manage external partners contracts budgets timelines and quality oversight.
- Provide advisory and operational support to allow scientific teams to focus on content and strategy.
- Support key service areas (e.g. planning & budgeting quality control external partner management lay project management technical writing) covering up to two areas simultaneously.
Educational Qualifications & Experience
Bachelors degree with a minimum of 35 years of working experience or comparable qualification preferably in e.g. business management data science in medicine pharmacy natural science medicine or digital technologies project management or communication science or any other relevant field with at least 3 years of professional experience preferably in clinical operations or related areas.
Years of experience refers to typical years of related experience needed to gain the required knowledge skills and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
Knowledge Skills Abilities:
Excellent data interpretation and medical writing skills including grammatical editorial and proofreading skills
Strong project management skills
Excellent interpersonal skills including problem solving
Strong negotiation skills
Excellent oral and written communication skills with strong presentation skills
Significant knowledge of global regional national and other document development guidelines
In-depth knowledge in a specialty area such as preclinical therapeutic regulatory submissions communications etc.
Great judgment and decision-making skills
Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel Outlook)
Working Conditions and Environment:
Work is performed in an office environment.
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 workplace where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.