Principal Medical Writer

Responsibilities

• Assist with researching, writing and editing clinical study reports and study protocols

• Summarize data from clinical studies

• Assist with more complex clinical, scientific and program-level documents such as IBs, INDs and MAAs

• Ensure compliance with quality processes for assigned documents

• Assist with program management activities such as timelines, budgets and forecasts

• Participate in project launch, review and team meetings

Requirements

• Bachelor's degree in a scientific discipline or equivalent

• Around 0 to 2 years of relevant experience

• Basic medical writing, grammatical, editorial and proofreading skills

• Ability to interpret and present complex data accurately and concisely

• Basic knowledge of regulatory documentation and drug development process

• Competent computer skills, including Excel and Outlook

Preferred Qualifications

• Experience in the pharmaceutical or CRO industry

• Experience in scientific writing

About the Company

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Its brands include Thermo Scientific, Applied Biosystems, Invitrogen and PPD.