Maharashtra

experience in teaching / research / industry out of which at least 3 years shall be at a post equivalent to that of an Associate Professor. Pharmaceutical Chemistry (with Pharmaceutical Analysis), Pharmaceutics, Pharmacognosy, Pharmacology, Pharmacy Practice & related subjects

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.

The selected candidates, who have passed JRF examination conducted by CSIR, UGC, ICMR, DBT can avail fellowship as per the rules of respective funding agency. Non-fellowship holders will be provided Institutional fellowship of Rs. 8000 per month only after successful completion of coursework and Ph.D. proposal presentation.

Postgraduate, Graduate degree in Science Eg. B.Pharm, Life Science, B.Sc., Biotech, Zoology, Botany, etc. with Diploma in Clinical Research is mandatory. One year experience in clinical trial monitoring is desirable.

research experience and knowledge in theoretical or computational biophysics, biophysical chemistry, protein dynamics, molecular dynamics simulations; Candidate should be familiar with enhanced sampling methods and MATLAB coding. Site-Specific Mechanism Of Aberrant Inter-Molecular Self-Assembly Of Full-Length TDP-43 In Neurodegeneration

Required Trial Coordinator under Resonance Research Capacity Building; Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. with PG Diploma in Clinical Research is mandatory. The Tata Memorial Centre, TMC is a Comprehensive Cancer Centre with a mission to achieve the highest standards in patient care, cancer prevention, cancer research and professional development for oncology and allied disciplines.

Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable

Experience working with Pharma-API plant. Responsible for adherence to SOP’s, to meet production targets, maintain safety practices. Able to handle and analyse process problems in manufacturing. Sound knowledge of operations of centrifuge, reactors etc.

Preparation of regulatory monitor and market intelligence data. Analyse and share market intelligence data and preparation of regulatory monitor capturing key regulatory developments on monthly basis.