Life Sciences

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.

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.

Hands-on experience in DNA sequence data analysis from FASTQ files, particularly on Human genomic or Metagenomic samples using standard data analysis pipeline. M.Sc / M.Tech in Life Science or experience in bioinformatic analysis of genomic/meta genomic data or Ph.D.in Life Science

M.Sc in Life Sciences, Chemistry from a recognized University or equivalent AND selected through a process described through anyone of the following National Eligibility Tests – CSIR-UGC NET including lectureship Assistant Professorship and GATE.

Bachelors degree in life sciences or business. Experience in consulting management in the life sciences, pharmaceutical/ biotech consulting industry or equivalent industry role

Post graduate degree in Life Science. OR Graduate, Post Graduate Degree In professional course e.g., M.Sc. Pharmacology, M.Pharm, MBBS,BDS selected through a process described through any one of the following Scholars who are selected through National Eligibility Test- CSIR-USG, NET including lectureship (Assistant Professorship) and GATE, GPAT.

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.