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A leading clinical research organization, MMS, is seeking a Principal Regulatory Strategist to provide consulting and advisory services for complex regulatory projects. The role requires a minimum of 15 years experience in Regulatory Affairs and offers the opportunity to work in a collaborative environment remotely, contributing to pioneering project outcomes within the pharmaceutical and biotech industries.
Are you looking to join a company where your contributions truly matter and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry-leading employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn.
This would be a full-time consultancy role working remotely.
Principal Regulatory Strategist Responsibilities
Requirements
Required Experience : Senior IC
Key Skills
Facilities Management, Attorney, Computing, Cardiovascular, Account Opening, Analytics
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