Key Tasks:
Requirement gathering in regarding to regulatory software development i.e. Pharmacovigilance (PV) Clinical Trial Management (CTM), further analysis work in the conjunction with software development team, sharing domain/subject knowledge with development team in regard to such complex regulatory solutions requirements, provide support to clients in the successful implementation of the regulatory software, user (clients) training, documentation, incorporate regulatory guidelines in the development of entire software, consult clients as subject matter expert to share software domain/subject related knowledge, educate clients through social media platform or webinars.
Keyskills: Training Social media Consulting Pharmacovigilance Subject Matter Expert Management
About Sarjen Systems; •High standard of Technology in partnership with Microsoft INC. •International ERP software development & implementation (S&D, Material Management, FICO, Production Planning, QM) •Best IT Company active in pharmaceutical sector. We have international pro...