Ph.D Biotechnology, Biochemistry, Bioinformatics or relevant branch of biological sciences with at least 1 research paper in Science Citation Indexed Journal.
Post Graduate Diploma in Clinical Trials or equivalent with at least 60% marks. At least one-year experience in clinical research. Experience in recruiting patients in clinical trials, familiarity with good documentation practices and good clinical practices.
Ability to conceptualize and drive large-scale marketing strategies with an execution-first approach. Experience in leading teams, collaborating with sales, and driving prescription demand at a national level.
Handling and Execution and investigation of QMS documents in change controls, deviations, and CAPA. Review of Analytical Method Validations, Method Transfers, Protocols & Reports. Experience in review of HPLC, GC, LCMS calibration data & Analytical Data review.
Diploma in Pharmacy D.Pharm or Bachelor of Pharmacy B.Pharm or Doctor of Pharmacy Pharm.D from a recognized University, Institution. Should be a registered Pharmacist under Pharmacy Act 1948.
Research experience in Drosophila genetics and epigenetics will be preferred. Masters degree in Natural or Pharmaceutical sciences and Three years of experience in Research and Development in industrial and academic institutions or Science and Technology organizations and scientific activities and services.
Project management for CoE-Antiviral and Antibacterial Drug Discovery and Development project and timely submission of progress reports to Director and nodal ministry. Proactively coordination of the project with various stakeholders and Principal Investigators of the project.
Doctoral Degree in Science, Engineering, Technology, Pharma from a recognized University or equivalent; Experience in Research & Development in Industrial & Academic Institutions or Science and Technology Organizations and Scientific activities and services
Experience of conducting and writing Systematic Reviews and Meta-analysis minimum two published systematic reviews as lead author. Knowledge about GRADE methodology. Experience in Statistics and Epidemiology
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