Apply Online for Associate Medical Writer at Thermo Fisher Scientific

Thermo Fisher Scientific Inc is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of 13 billion USD, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. We create value for our key stakeholders through three premier brands, Thermo Scientific, Fisher Scientific and Unity™ Lab Services, which offer a unique combination of innovative technologies, convenient purchasing options and a single solution for laboratory operations management.

Post : Associate Medical Writer

Job Description
• Assists with researching, writing, and editing routine documents including Informed consent forms, Lay summaries, and other patient centric documents.
• May assist with more complex clinical and scientific and program level documents.
• 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.

Candidate Profile
• 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 1 to 3 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)

Additional Information
Experience : 1 to 3 years
Qualification : Bachelor's degree
Location : Mumbai, Maharashtra
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical Research
End Date : 31st August 2026