Responsible to monitors activities at clinical study sites to assure adherence to Good Clinical Practices GCPs, Standard Operating Procedures, and study protocols under supervision of Clinical Operations Manager, Clinical Research Specialist.
Investigation on the Cohesive Roles of Glycogen Synthase Kinase 3 alpha and FTO in Regulation of Mammalian Spermatogenesis. M.Pharm., with first class and a minimum of 1 year of research experience after obtaining the highest degree.
Ph.D. from a recognized University in subject as given in a subject related to Reproductive, Child Health and Nutrition Experience of having worked in the area of management of reproductive health problems.
Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry. Within a decade since inception in 2007, Biophore has emerged as a trusted partner in the generic industry across US, Europe and other regulated markets.
Master’s Degree in Chemistry or Pharmaceutical Chemistry or Pharmaceutical Analysis, Quality Assurance from a recognized University or equivalent. Working expertise in HPTLC, HPLC, ICP- OES and Plant based Drug Standardization, Analysis of Aflatoxin & Pesticide residue. Skills of drafting and editing of scientific documents, technical reports
Candidates having prior experience in plant-soil- microbial interactions, soil microbiology and microbiome analysis metagenomics, microbial screening, cultivation, characterization and enrichment studies, pathway/mechanisms analysis, microbial consortia development, state-of-the art molecular biology techniques, and detection of xenobiotics and secondary metabolites, LC-MS, GC- MS are encouraged to apply.
M.Sc, Microbiology, Biotechnology, Zoology, Botany from a recognized university or M.Sc. in life Sciences, Zoology, Botany, Marine Sciences, Chemistry, Environmental Sciences from a recognized university or equivalent.