ACTREC

To work on project entitled Biobanking in Multiple Myeloma. Graduation or Post Graduation degree in Science with PG Diploma in Clinical Research is mandatory.

The candidate must have experience using analytical techniques like ICP- MS/ HPCL/ LC-MS/ GC-MS with a hands- on experience in handling Biological samples. Desirable 5 years research, teaching and design and development experience after M.VSc, M.Pharma, ME, M.Tech, M.Sc Life science, Biotechnology. One research paper in Science Citation indexed SCI Journal is Desirable.

Working in a state-of-the-art pharmacology and experimental therapeutics laboratory, the candidate will lead a small group of passionate researchers in the discovery and development of herbal drugs for cancer through design and conduct of experiments, conducting regular team meetings, preparation of progress reports and any other work assigned by the Principal Investigator.

Masters degree in Life Science, or equivalent with at least 60% marks. Experience in IP management, patent drafting, certification in IPR will be preferred. Prior art search, good organizational skills, strong written and verbal communication skills and basic computer knowledge are desirable.

Basic & Translational Research in Cancer; Post graduation in M.Pharma, Life Sciences, Biotech, zoology, Botany with PG Diploma in Clinical Research-Mandatory. To work on project entitled Basic and Translational Research in Cancer.

Graduation in Biotechnology or B.Pharmacy from Govt. recognized University and Boards. Computer course in office software. Knowledge of Biostatistics. Research Methodology workshop training and Good clinical laboratory Practices

Ph.D. in the area of Life Sciences, Chemical Sciences, Physical Sciences or interdisciplinary areas. Experience with Semi-thin and ultra-thin sectioning using ultra-microtome. Providing training to the students and other researchers for the use of Electron Microscopy facility for research projects.

Mechanisms that govern spontaneous humoral immune responses at tumor beds and outcome. M.Sc, M.Tech in any branch of Life Sciences.

PG in Science M.Pharm, M.Sc. in Life Science, Clinical Research Regulatory Affairs with 65% plus Diploma in Clinical Research and Pharmacovigilance Activity from recognized university. 1 years’ experience in Clinical research or IEC management is mandatory.