Senior Medical Writer — Regulatory Submissions Leader

With its beginnings in a family run pharmacy in Correggio, Italy in the ****s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn.We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors...

A leading biopharmaceutical solutions company is looking for a Principal Medical Writer to develop regulatory documents for global submissions.This role entails managing writing projects, collaborating with cross-functional teams, and ensuring compliance with global guidelines.The ideal candidate will have experience in regulatory writing and a solid...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating...

A leading medical technology company in Milan seeks a Clinical Evaluation Medical Writer to analyze clinical evidence supporting regulatory submissions.The role requires strong technical writing skills and proficiency in clinical research to ensure comprehensive literature reviews.Successful candidates will be well-versed in FDA regulations and able to work...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating...

MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating...

A leading medical technology company in Milan seeks a Clinical Evaluation Medical Writer to analyze clinical evidence supporting regulatory submissions.The role requires strong technical writing skills and proficiency in clinical research to ensure comprehensive literature reviews.Successful candidates will be well-versed in FDA regulations and able to work...