Medical Writer - Medical Information

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Medical Writer - Make an Impact at the Forefront of Innovation The Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence. What You'll Do: Serve 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. May assist with more complex clinical and scientific and program level documents, including IBs, INDs, and MAAs. Ensure compliance with quality processes and requirements for assigned documents. May assist in determining best practices, methods and techniques for achieving optimal results. May assist in program management activities. Duties could include assisting with developing timelines, budgets, and forecasts for assigned deliverables. Represent the department at project launch meetings, review meetings, and project team meetings. Education & Experience Requirements: Bachelor's 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 2+ years). Experience working in the pharmaceutical/CRO industry preferred Experience in scientific writing advantageous Knowledge, Skills, Abilities: Solid 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 tea Effective oral and written communication skills Good knowledge of regulatory documentation and drug development process Great judgment and decision-making skills Good computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook) 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. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs. Compensation and Benefits The salary range estimated for this position based in Massachusetts is $100,000.00–$120,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards