for use across Achilles clinical trial programmes. This role will play a key part in establishing, growing, and maintaining the quality... requirements relating to clinical trial manufacture are met and maintained for ATIMPs (Advanced Therapy investigational Medicinal...
Achilles TherapeuticsMMS 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. Strong industry experience...
MMSMMS 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. Strong industry experience...
MMS HoldingsMMS 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. Strong industry experience...
MMSMMS 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. Strong industry experience...
MMSMMS 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. Strong industry experience...
MMSdevelopment, including knowledge of applicable clinical trial safety regulations and postmarketing safety regulations. Includes...Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so...
Randstad(Investigational Medicinal Product), thereby ensuring GxP and other regulatory requirements relating to clinical trial manufacture... and its Review Desirable: Understanding of Clinical Trial Directives/Regulations Knowledge about Regulatory Requirements...
Achilles Therapeutics