At Thermo Fisher Scientific, you will engage in meaningful work that positively impacts global health. Join our mission to make the world healthier, cleaner, and safer. Our teams are equipped with the resources needed to achieve personal career goals while advancing scientific research and delivering life-changing therapies. With clinical trials conducted in over 100 countries, we are continually developing new frameworks for clinical research. Your commitment to quality and accuracy will enhance health outcomes worldwide.
Summarized Purpose:
Medical Writer (Remote, India)
Job Id: R-01242044
Job Type: Full-time
Category: Clinical Research
Remote: Fully Remote
We are expanding our India Medical Writing FSP Team and seek a dedicated Medical Writer. Experience in Immunology, Oncology, or Vaccines is advantageous but not essential. The role involves producing high-quality medical and scientific writing from planning to the delivery of final drafts for internal and external clients. You will support effective communication, ensuring operational excellence.
Essential Functions:
- Serve as the primary author for routine documents such as clinical study reports and protocols.
- Summarize data from clinical studies and assist with complex clinical and scientific documents, including IBs, INDs, and MAAs.
- Ensure compliance with quality processes and requirements.
- Assist in determining best practices for achieving optimal results.
- Support program management activities, including developing timelines, budgets, and forecasts.
- Represent the department in project launch, review, and team meetings.
Education and Experience:
- B.Pharm, M.Pharm, Msc. BSc, Pharm.D, Lifesciences
- 2+ years of relevant experience.
- Pharmaceutical/CRO industry experience preferred.
- Experience in scientific writing is advantageous.
- Knowledge in Immunology, Oncology, or Vaccines is a plus.
Knowledge, Skills, and Abilities:
- Strong medical writing skills, including grammar, editing, and proofreading.
- Ability to accurately interpret and present complex data.
- Excellent administrative, organizational, and planning skills.
- Detail-oriented with a commitment to quality.
- Ability to work independently and as part of a team.
- Effective communication skills, both oral and written.
- Good understanding of regulatory documentation and the drug development process.
- Strong decision-making and judgment skills.
- Proficient in using document management systems and relevant applications (e.g., Excel, Outlook).