Bangalore

Offers leadership and basic accountability, provides strategic assistance, and planning support for clinical regulatory documents. Writers and edits clinical regulatory documents, including submission summaries and other complex documents.

Ensures that direct reports have development and training plans, according to IDP process. Coaches the direct reports on a regular basis, and plans, organizes coaching with external providers if needed.

Perform complex scientific study data review and management of CDM, Study Responsible Scientist SRS, and Study Responsible Physician related queries in EDC system. Involvement in other clinical data review activities e.g., Coding, SAE reconciliation is possible.

First class Post Graduate Degree, including the integrated PG degrees. Second class Post Graduate Degree, including the integrated PG degrees, with PhD. Development and characterization of a novel silk fibroin-based hydrogel loaded with recombinant human parathormone for osseous regeneration and evaluation of its efficacy in murine models

Candidate should have knowledge of theoretical working principle of KF auto titrator, dissolution, spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC 

Masters degree in Life sciences or Biotechnology; Experience in 2D cell culture, stem cell science, and 3D cell culture techniques. Experience in scientific writing.

Knowledge of ASU drug standardization and analytical techniques. Handling analytical instruments like HPTLC, HPLC, etc. Drafting of scientific documents/ research articles/ technical reports etc., Working knowledge of computer applications. Master of Science M.Sc. in Chemistry/Analytical Chemistry or Master of Pharmaceutical Sciences M.Pharma

Dual functional COX-2 inhibiting and antimicrobial NSAID-peptidomimetic conjugates as novel therapy to tackle septic infections. Ph.D, MD, MS, MDS or equivalent degree OR three years of research, teaching, design and development after MVSc, M.Pharm, M.E, M.Tech with at least tree research papers in high impact Journals. Candidates having research experience in organic synthesis, peptide synthesis, purification and characterization will be preferred.

Develop strategy to configure, distribute, and collect, and review and approve, high quality country specific and or site specific documents or essential regulatory documents and any updated or amended regulatory documentation.