Mms Holdings Inc. Jobs In VA - 7
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Principal Clinical Data Manager (remote)
- @ MMS Holdings Inc.
- San Jose, CA
- Fulltime
- 3 years ago
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 -
Principal Clinical Data Manager (remote)
- @ MMS Holdings Inc.
- Jacksonville, FL
- Fulltime
- 3 years ago
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 -
Principal Clinical Data Manager (remote)
- @ MMS Holdings Inc.
- San Diego, CA
- Fulltime
- 3 years ago
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 -
Principal Clinical Data Manager (remote)
- @ MMS Holdings Inc.
- Baltimore, MD
- Fulltime
- 3 years ago
MMS 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 -
Principal Clinical Data Manager (remote)
- @ MMS Holdings Inc.
- Princeton, NJ
- Fulltime
- 3 years ago
MMS 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 -
Global Regulatory Affairs Manager
- @ MMS Holdings Inc.
- Miami, FL
- Fulltime
- 3 years ago
MMS is an award-winning, data-focused CRO that supports the pharmaceutical and biotech industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong -
Manager, Biostatistics (remote)
- @ MMS Holdings Inc.
- United States
- Fulltime
- 3 years ago
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