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MMS is a award-winning, data-focused clinical research organization (CRO). Expertise within CROs and scientific and clinical data/ terminology, and the drug development process. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges.
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Monitor vendors and clinical investigator sites to ensure processes are followed and quality is maintained independently. Assists in other duties relating to overall compliance within Quality and Compliance department, as requested.
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Join us at MMS and be part of a team that is shaping the future of clinical research. 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.
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Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn. Job Specific Skills:Maintains a strong understanding of regulations and guidance as they pertain to compliance; maintains knowledge relating to regulatory updates.
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Must be willing to travel up to 20% of the time for client work within the US.Requirements:College graduate in scientific, medical, clinical discipline or related experience; or minimum of 7 years experience in GCP regulated industry if not a college graduateMinimum of 5 years experience in GCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.
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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.
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Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards.
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With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO in Global Health & Pharma’s international awards programs for the last three consecutive years.
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Minimum of 5 years’ experience in GCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.) College graduate in scientific, medical, clinical discipline or related experience, Masters preferred; or minimum of 7 years’ experience in GCP regulated industry if not a college graduate.
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Mmsholdings.com or follow MMS on LinkedIn. Experience in reviewing and editing QMS related documents, i.e., SOPs, Work Practices, Forms, Training Materials, etc. Develop CAPA plans and contribute to resolution of audit findings independently.
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Requirements: College graduate in scientific, medical, clinical discipline or related experience, Masters preferred; or minimum of 7 years’ experience in GCP regulated industry if not a college graduate Minimum of 5 years’ experience in GCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.
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Understanding of how to plan, prepare and conduct GCP audits independently. Hands-on experience with clinical trial and pharmaceutical development preferred. Must be willing to travel up to 75% of the time for audits within the US and potential travel to Canada.
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Comor follow MMS onLinkedIn. College graduate in scientific, medical, clinical discipline or related experience; or minimum of 7 years’ experience in GCP regulated industry if not a college graduate.
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Must be willing to travel up to 20% of the time for client work within the US. Proficient with 21 CFR Part 11, FDA, and GxP requirements. We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate.
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Maintains a strong understanding of regulations and guidance as they pertain to compliance; maintains knowledge relating to regulatory updates. Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team.
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data quality jobs Title: quality specialist Company: Mms
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