Clinical Medical Writer

Welcome to Sanofi, a global biopharmaceutical company committed to improving lives through innovative medical solutions. We are currently seeking a highly skilled Clinical Medical Writer to join our dynamic team. As a Clinical Medical Writer at Sanofi, you will play a crucial role in translating complex scientific data into clear and concise medical communications. Your expertise will contribute to the development of life-changing treatments and therapies for patients around the world. To excel in this role, you must possess a strong background in scientific writing, exceptional attention to detail, and a passion for improving healthcare outcomes. If you are ready to make a meaningful impact in the medical field, we invite you to apply for this exciting opportunity at Sanofi.

1. Translate complex scientific data: The Clinical Medical Writer will be responsible for translating complex scientific data into clear and concise medical communications, including clinical study reports, scientific publications, and regulatory documents.
2. Contribute to the development of life-changing treatments and therapies: The writer will play a crucial role in contributing to the development of new treatments and therapies for patients around the world by effectively communicating the scientific data and findings.
3. Ensure accuracy and precision: The writer must have exceptional attention to detail and be able to ensure the accuracy and precision of all medical communications to maintain the integrity of the data and findings.
4. Collaborate with cross-functional teams: The writer will work closely with cross-functional teams, including clinical researchers, regulatory affairs, and medical affairs, to gather and synthesize scientific information and data.
5. Stay updated on industry trends and regulations: The writer will be responsible for staying updated on the latest industry trends and regulations related to medical writing to ensure all communications are compliant and of high quality.
6. Write and review medical documents: The writer will be responsible for writing and reviewing various medical documents, including clinical trial protocols, study reports, manuscripts, and regulatory submissions, to ensure they meet internal and external standards.
7. Meet deadlines: The writer must be able to manage multiple projects and meet tight deadlines while maintaining a high level of quality and accuracy.
8. Adhere to company and industry guidelines: The writer must adhere to company and industry guidelines, such as Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH), when writing and reviewing medical documents.
9. Collaborate with external partners: The writer may also collaborate with external partners, such as key opinion leaders and medical writers from other organizations, to ensure the accuracy and consistency of medical communications.
10. Contribute to continuous improvement: The writer will be responsible for contributing to the continuous improvement of medical writing processes and procedures to enhance efficiency and quality.
11. Uphold company values: The writer must uphold

According to JobzMall, the average salary range for a Clinical Medical Writer in Budapest, Hungary is between 3,700,000 HUF to 7,000,000 HUF per year. This equates to approximately $13,500 to $25,500 USD per year. However, salaries can vary depending on factors such as experience, education, and specific job responsibilities.

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.