About MMS
We are a data-focused clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries. We offer services in clinical strategy and execution, regulatory affairs and submissions, clinical programming and biostatistics, data management, clinical trial disclosures, medical writing, GCP auditing, use of Real World Evidence, pharmacovigilance and drug safety, quality control, quality assurance, and data science. We provide full-service biometrics solutions, regulatory submission support from the Investigational New Drug (IND) application stage through New Drug Applications (NDA), and safety and risk management from Phase 1 through post-approval. We have therapeutic expertise in areas such as rare diseases, psychedelics, oncology and radiopharmaceuticals, and central nervous system (CNS) disorders. We also offer a Functional Service Provider (FSP) model.
Our key technologies include:
- KerusCloud® simulates and analyzes trial scenarios to optimize endpoints, recruitment strategies, and overall trial design.
- Datacise® analyzes and visualizes clinical data, Real-World Data (RWD), and other data sources. It supports IDMC management, safety signal detection, and data flow management.
- PVantage® is a pharmacovigilance adverse event management platform that streamlines and automates case processing activities.
- Automatiqc® is an AI, cloud-based application designed to aid in document authoring for medical and regulatory writing.
We were founded in 2006 and operate globally across four continents. Over the past five years, we’ve supported more than 50 marketing applications and consistently receive high customer satisfaction ratings.
Mission & Values
Our mission is to deliver high-quality service and technology solutions, rooted in strong science and decades of regulatory experience, that will assist clients in developing and marketing life-changing therapies to positively improve lives worldwide.
Our values include:
- Strive for Good Science and Strong Processes We are committed to making sound decisions based on scientific principles, internal expertise, and applicable regulation. We emphasize strong internal processes to ensure high-quality deliverables.
- Value Talent – Find, Attract, Enhance and Retain We recognize that talented staff drives our business. We focus on identifying and attracting top talent, continuous training, and fostering enthusiasm, collaboration, and teamwork within a global and diverse talent pool.
- Wow the Customer We aim to deliver value that exceeds expectations, maintaining a customer focus throughout the project lifecycle to build trust and long-term relationships.
- Bring a Sense of Urgency and Leadership (SOUL) We promote the importance of SOUL through a healthy work environment. We ensure project work is completed on time, identify risks and solutions proactively, and encourage colleagues to take responsibility for project success.
Team & Culture
We have a global team of over 950 colleagues, with our company size between 501-1000 employees. We foster a collaborative and inclusive culture. Our culture is described as science-driven, customer-driven, dependable, flexible, and agile, with a focus on consistent staff and proactive solutions. We have been recognized as a Top Workplace in the United States and Michigan for two consecutive years, and as a Certified Great Place to Work in India. We emphasize a culture where colleagues become invested in a sponsor’s project, guiding them towards positive outcomes.
Frequently Asked Questions
MMS provides full-service biometrics, regulatory submissions, safety and risk management, therapeutic expertise, and Functional Service Provider (FSP) models. They offer AI-enabled technology platforms like KerusCloud® for trial simulation, Datacise® for data visualization and analysis, PVantage® for pharmacovigilance, and Automatiqc® for medical and regulatory writing.
MMS fosters a collaborative and inclusive culture. It is described as science-driven, customer-driven, dependable, flexible, and agile, with an emphasis on taking responsibility for project success. MMS has been recognized as a Top Workplace in the United States and Michigan, and a Certified Great Place to Work in India.
MMS brings specialized knowledge in rare diseases, psychedelics, oncology and radiopharmaceuticals, and central nervous system (CNS) disorders, among others.
MMS was founded in 2006.
MMS is active in the Clinical Strategy & Execution, Regulatory Affairs And Submissions, Clinical Programming & Biostatistics, Data Management, Clinical Trial Disclosures, Medical Writing, Gcp Auditing, Clinical Research Organization, Use Of Real World Evidence, Pharmacovigilance & Drug Safety, Quality Control, Quality Assurance, and Data Science markets.
MMS has 501-1000 employees.
MMS hires in 🇬🇧 United Kingdom, 🇺🇸 United States, and 🇿🇦 South Africa.
MMS is not actively hiring at the moment. Check back later for new opportunities.
Yes, MMS is a remote-first company.
MMS's website is www.mmsholdings.com .
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