Perform data profiling and validation tasks across multiple clinical data sources to identify data quality issues and anomalies within Clinical data i..Share
Candidates main focus is to address and maintain the quality of all processes/methods, materials and equipment to be used at the Northbridge Facility...Share
Recommend / identify / facilitate agreeing on data standards for new RIMS and data migration naming convention, reference data standards, master data..Share
This person will be responsible for leading, conducting, and owning risk management activities including hazard analysis, system risk analysis, and va..Share
We are currently hiring professionals and entrepreneurs who can provide specialized guidance and advice for clients in the areas of investment and ins..Share
Packaging systems, medical device class II and III, design verification and validation experience for primary, secondary and tertiary; flexible and ri..Share
Candidates for this work-from-home position must be 21 or older, have an SSN, own a personal computer, and reside in New Jersey, Pennsylvania, Michiga..Share
Scientific and analytical evaluation skills US FDA medical device regulations, standards, and guidance. Provides RA support for change control project..Share
Junior Associates! Have you ever wanted to practice HEALTH CARE LAW but didn' t know how to begin? Our client, an established and premier Health Care ..Share
Introduction Axtria is a leading global provider of cloud software and data analytics to the Life Sciences industry. We help Life Sciences companies t..Share
Seeking motivated individuals to participate in National Focus Groups and Clinical Trial studies. Earn up to $750/week in your spare time. Must regist..Share
Recommend / identify / facilitate agreeing on data standards for new RIMS and data migration naming convention, reference data standards, master data..Share
Manage execution / authoring and review of CMC documentation (Module 1 , 2 and 3 / Part II ) for life cycle management - post-approval supplements, ba..Share
You should have excellent understanding of 21 CFR Part 11, ICH standards, EMA and FDA (GxP) regulations, and GAMP methodologies. Review and Pre-Approv..Share