Job Description
MM S is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. 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.
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. For more information, visit www.
mmsholdings.com or follow MMS on LinkedIn (https://www.
linkedin.com/company/mms-holdings-inc-/) .
This is a project-based consulting position. Responsibilities: + Plan and conduct GCP audits in the Medical Device,...
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. For more information, visit www.
mmsholdings.com or follow MMS on LinkedIn (https://www.
linkedin.com/company/mms-holdings-inc-/) .
This is a project-based consulting position. Responsibilities: + Plan and conduct GCP audits in the Medical Device,...