Karnataka

B.Pharm, M.Pharm, Pharm.D or BDS.; Working knowledge of literature case processing, drug safety regulations and adverse event reporting

Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech, Client SOPs. 

M.Sc, M.Tech, M.Pharm with prior experience in Quality Assurance with 5-10 years in GMP pharmaceutical organization

M. Pharm with 10 years of experience in handling ADME assays and HPLC and LCMS, MS Or Fresh Ph.D. in similar disciplines

Ph.D. in relevant discipline and M.Pharm Pharmaceutical Quality Assurance, experience and good track record of publications, patents. The candidates who have submitted PhD thesis may also apply.

The individual has experience in handling various analytical techniques such as such as HPLC, GC, CE-SDS, SEC, ELISA, qPCR, DSC, Bioassay, Karl Fischer, UV, LC-MS, Dissolution, Disintegration, X-ray diffraction, etc.

Informing customers about the required documents for processing the customer orders. Sending reminders to the customer. Review and archive the documents from the customer.

Masters degree in pharmacy, life sciences, biotechnology is required. At least 1 year in healthcare company analysis, market research, or US market access, knowledge of US healthcare marketplace and government programs such as Medicaid, Medicare etc

Propose staff and provide CVs for potential projects, following agreement of applicable functional counterparts e.g. CRA Managers or CTM Directors, focusing on the skill sets required by the Sponsor and the availability during the timeframe of the study