Life Sciences

experience in drafting, filing and prosecution of Patent applications in India, coordinating with legal teams, advising clients on IP strategy and monitor compliance. Experience in performing comprehensive patent searches in curated database to identify relevant prior art and assess patentability.

Assessing the theranostic capabilities of the Aurora-A/TPX2 Complex in Gallbladder Cancer; MSc/ MTech in Life Sciences, Biotechnology, Biochemistry, Microbiology, Toxicology, Molecular oncology, Bioinformatics, Molecular Oncology, and Genetics with two years of research experience in Biochemistry/Biotechnology/Immunology/Molecular Biology. The candidate should have a valid UGC-CSIR NET/ GATE/ GPAT/ DST/ DBT/ DAE/ DOS/ DRDO/ MHRD score.

Towards Discovery and Development of Novel Drugs and Pharmaceuticals. Experience in Natural Product Isolation and Characterization, Evident from Publication. Organic Synthesis, Natural Product Isolation, HPLC analysis.

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.

Delineating and characterizing the m6A RNA methylation marks in primary and relapsed B-cell Acute Lymphoblastic Leukemia; MSc Life Sciences research experience or PhD in life sciences; Hands on research experience in molecular biology experiments PCR, Real Time PCR, Cloning, bioinformatics analysis of transcriptomes, exomes, custom analysis is desirable.

A multi-omics approach to delineate the role of neutrophil and plasma indicators in the progression of sepsis and predisposition to early mortality in Severe Alcoholic Hepatitis, SAH Patients. First class post graduate degree including integrated PG degrees

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

PhD in any branch of Life Sciences from a recognised University. Work experience in the area of Virology, Cell culture and immunological assays. Live virus handling and neutralization assay. Experiences in doing DNA cloning, protein purification, western blots, FACS experiments and biophysical techniques. The candidates should also have experience in handling animals. Doctoral degree in Science/ Pharma

Functional implications of the PPARs and TLRs in the pathophysiology of ischemic stroke activation mediated downstream signaling cascade. Postgraduate Degree, including the integrated PG degrees in Biophysics/ Biotechnology/ Molecular Biology/ Biochemistry/Computational Biology & Bioinformatics Life Sciences from a recognized University.