
Medical Regulatory Writer
Are you a skilled writer with a passion for healthcare and a strong attention to detail? Look no further! Sanofi is seeking a talented Medical Regulatory Writer to join our team. In this role, you will play a crucial role in ensuring the accuracy and compliance of our medical documents and submissions. As a member of our team, you will have the opportunity to work with cross-functional teams and contribute to the development of life-changing treatments for patients. We are looking for a motivated individual with excellent communication skills and a background in medical writing or a related field. If you are ready to make a meaningful impact in the pharmaceutical industry, we would love to hear from you!
- Write high-quality, accurate, and compliant medical documents and submissions for Sanofi's pharmaceutical products.
- Collaborate with cross-functional teams, including regulatory, medical, and clinical teams, to gather necessary information and ensure the accuracy of medical documents.
- Review and edit documents to ensure they adhere to regulatory guidelines, company standards, and industry best practices.
- Conduct thorough research and analysis on medical and scientific information to support document development.
- Utilize strong attention to detail to identify and correct any errors or inconsistencies in medical documents.
- Stay up-to-date on industry regulations and guidelines to ensure compliance in all written materials.
- Communicate effectively with team members and stakeholders to ensure timely completion of projects.
- Contribute to the development and improvement of internal processes and templates for medical writing.
- Maintain confidentiality and adhere to ethical standards when handling sensitive medical and scientific information.
- Demonstrate a strong understanding of medical terminology and the ability to translate complex scientific information into clear and concise language.
- Meet tight deadlines and handle multiple projects simultaneously.
- Continuously strive for excellence in all written materials and contribute to the overall quality of Sanofi's medical documents.
Bachelor's Or Advanced Degree In A Relevant Scientific Field Such As Biology, Pharmacy, Or Medicine.
Minimum Of 3-5 Years Of Experience As A Medical Writer In The Pharmaceutical Industry, Preferably With A Focus On Regulatory Writing.
In-Depth Knowledge Of Ich And Fda Guidelines For Clinical Trial Documentation, As Well As A Strong Understanding Of Global Regulatory Requirements.
Excellent Writing Skills With The Ability To Effectively Communicate Complex Medical And Scientific Information In A Clear And Concise Manner.
Familiarity With Document Management Systems And Experience In Managing And Coordinating Multiple Writing Projects Simultaneously.
Data Analysis
Clinical Research
Writing Skills
Drug development
Regulatory compliance
FDA regulations
Scientific Communication
Project
Clinical Trials
Medical Writing
Regulatory Submissions
Pharmaceutical Industry
Communication
Conflict Resolution
Leadership
Time management
Interpersonal Skills
creativity
Attention to detail
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Medical Regulatory Writer in Hyderabad, Telangana, India is between ₹3,00,000 - ₹5,00,000 per year. However, this can vary depending on the specific job role, company, and individual qualifications and experience. Some Medical Regulatory Writers may earn higher salaries, up to ₹8,00,000 per year, while others may earn lower salaries, around ₹2,00,000 per year.
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Sanofi SA is a French multinational pharmaceutical company headquartered in Paris, France, the world's fifth-largest by prescription sales. Building a More Equitable Future through Inclusive Clinical Trials · Rethinking the science of COPD · Grassroots Manufacturing Solutions for a Healthier Planet.

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