MMS is a leading data-focused Contract Research Organization (CRO) specializing in pharmaceutical and biotechnology innovation. With a strong emphasis on regulatory expertise and technological innovation, MMS provides a comprehensive range of services including regulatory submissions, data management, biostatistics support, medical writing, and pharmacovigilance. The company is known for its AI and technology-driven platforms like Datacise®, PVantage®, and Automatiqc®, which enhance efficiency and streamline clinical trial processes. MMS supports its clients from the investigational new drug application phase through to marketing authorization and post-approval, offering integrated solutions to accelerate drug development and mitigate risks. Recognized as a top workplace and for leadership in ESG sustainability, MMS is committed to empowering its employees and driving successful outcomes for its clients on a global scale.
Clinical Strategy & Execution • Regulatory Affairs and Submissions • Clinical Programming & Biostatistics • Data Management • Clinical Trial Disclosures
August 30, 2023
🇺🇸 United States – Remote
💰 Private Equity Round on 2022-06
⏰ Full Time
🟠 Senior
✏️ Content Writer
🦅 H1B Visa Sponsor
August 30, 2023
🇬🇧 United Kingdom – Remote
💰 Private Equity Round on 2022-06
⏰ Full Time
🟠 Senior
🇬🇧 UK Skilled Worker Visa Sponsor
August 30, 2023
🇬🇧 United Kingdom – Remote
💰 Private Equity Round on 2022-06
⏰ Full Time
🔴 Lead
🇬🇧 UK Skilled Worker Visa Sponsor
August 30, 2023