Senior Medical Writer

Work Schedule

Standard (Mon-Fri)

Office

Join Us as a Senior Medical Writer – Make an Impact at the Forefront of Innovation

Provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. Demonstrates subject matter and therapeutic area expertise. May function as a project lead. Collaborates with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

• Serve as primary author who writes and provides input on routine documents such as Medical Information Response Documents and Questions and Answers.
• May research, write or edit complex clinical and scientific and program level documents, including AMCP dossiers and Infographics.
• Review routine documents prepared by junior team members. May provide training and mentorship for junior writers on document preparation, the use of software for document development, document types, and therapeutic area knowledge.
• Ensure compliance with quality processes and requirements for assigned documents. Provide input on and independently develops best practices, methods and techniques for achieving optimal results, including various client specific processes.
• May function as a project lead or assist with program management activities. Duties could include developing timelines, budgets, forecasts, and contract modifications; tracking deliverable metrics; and representing medical writing team in client meetings.

• Bachelor’s degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification;
  Advanced degree preferred
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5 years).
• Experience working in the pharmaceutical/CRO industry preferred
• Additional qualifications in medical writing or medical information advantageous

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.

• 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)

• 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.

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

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.