General oversight for the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial....
The CRA conducts monitoring visits for assigned protocols and study sites. Overall responsibilities are to ensure that the study is being conducted in...
Engage in client communications for all important functions including data understanding/ exploration, strategizing solutions etc. 5 to 8 Years of experience....
Program Management, Process Consulting, IT Strategy, Portfolio Rationalization, Customer Experience with respect to Regulatory Affairs value chain,What will you...
By creating an Indeed Resume, you agree to Indeeds Terms of Service, Cookie Policy and Privacy Policy, and agree to be contacted by employers via Indeed. You consent to receiving marketing messages from Indeed and may opt from receiving such messages by following the unsubscribe link in our messages, or as detailed in our terms.
Teva Pharmaceuticals is committed to equal opportunity in employment. Teva is a global pharmaceutical leader and the worlds largest generic medicines producer,...
Indegene is a leading provider of R&D, commercial and marketing solutions to global pharmaceutical and healthcare organizations. ABOUT THIS COMPANY....
Proactively pursue to increase own business understanding of Novo Nordisk and the pharmaceutical industry. You need to plan own work and in co-operation with...
Maintain knowledge of relevant Quality System Regulations and safety requirements while building knowledge of other regulatory requirements related to R&D ...
Review of clinical study data base design and medical coding. Review of electronic case report form specification, edit check specification, UAT plan & report...
