
501 - 1000 employees
💊 Pharmaceuticals
🧬 Biotechnology
☁️ SaaS
💰 Private Equity Round on 2022-06
Pharmaceuticals • Biotechnology • SaaS
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.
🕒 April 21
🇬🇧 United Kingdom – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
✍️ Designer
🇬🇧 UK Skilled Worker Visa Sponsor
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501 - 1000 employees
💊 Pharmaceuticals
🧬 Biotechnology
☁️ SaaS
💰 Private Equity Round on 2022-06
Pharmaceuticals • Biotechnology • SaaS
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.
• Develop intellectual property and assets to support the design and analysis of clinical trials, precision medicine and real-world data analytics. • Address the emerging analytics needs of the Industry with biostatistics services, bespoke algorithms and proprietary trial simulation software KerusCloud. • Assist customers with their study design focusing on simulation with KerusCloud. • Prepare study protocols and develop Statistical Analysis Plans and Reports. • Summarize, analyze and visualize study data using statistical methods, delivering results to agreed timelines. • Provide statistical consultancy support to sponsors across clinical development, overseeing third-party deliverables. • Maintain knowledge of relevant research techniques and participate in continuous professional development. • Support pre-sales discussions to understand client needs, contributing to technical solutions and estimates. • Collaborate with Product Development team on statistical aspects of KerusCloud.
• Bachelors degree in mathematics, statistics, physics, pharmacology or with a strong statistical component, Masters or PhD preferred. • 5-7 years of experience in the application of medical statistics (pharma, CRO, academic). • Willingness to engage with clients to understand and research problems and provide creative, business-orientated solutions. • Experience in delivering customer projects to high quality standards. • Experience in SAS and/ or R statistical software packages. • Experience in study design and protocol and report-writing preferred. • Experience of modelling and simulation techniques to explore complex study designs preferred. • Experience of Bayesian approaches to design and analysis of clinical data preferred. • Experience of early-phase drug development processes including innovative/ adaptive study design preferred.
• Continuous professional development activity • Supportive, innovative team environment • Opportunity to shape the future of clinical research
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