About MMS: 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).

Do you have the skills to fill this role Read the complete details below, and make your application today. 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 maintains an industry-leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn. This would be a full-time role, working remotely. Job Responsibilities: Possesses high-level knowledge of drug development as it pertains to biometrics. Stays current with the latest industry practices and updated regulatory guidelines. Understands the various tools we work with and can use them correctly (e.g., checks in/out; Power BI for dashboard development; SharePoint). High technical level, Subject Matter Expert in biometrics; willing to guide others in biostatistical techniques. Proficient in understanding regulations and guidance related to data-centric deliverables; mentors others and advises on industry trends and technologies. Ability to define and implement new methods, tools, and solutions to meet stakeholder needs. Proficient in conducting peer reviews and validation of project deliverables. Maintains a strong understanding of industry trends and technologies in Biometrics. Job Requirements: College degree in statistics or related field; master's or PhD preferred, or extensive relevant experience. Minimum of 12 years’ experience in Biometrics or a similar field. Ability to anticipate and resolve potential client-related problems. Demonstrates managerial skills and experience. Proficiency with MS Office; experience with clinical trials and pharmaceutical development preferred. Good communication and problem-solving skills; ability to work collaboratively. Familiarity with ISO 9001 and ISO 27001 standards preferred. Knowledge of 21 CFR Part 11, FDA, and GCP requirements. Basic understanding of CROs, clinical data, and drug development processes. Powered by JazzHR

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