Post Graduates in Life Sciences, Pharmacy, Statistics, Social Works, Sociology, BAMS, BSMS, with MD in AYUSH to support Intramural Primary Research co- ordination and facilitate in better central procurement planning framework at ICMR headquarters
M.Sc in Zoology, Biochemistry, Botany, Molecular Biology, Biotechnology, Microbiology, Life Science from a recognized University or M.Sc in Forensic Science
Post-Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany etc, with PG Diploma in Clinical Research is Mandatory. Experience Desirable, in handling multicenter projects.
Masters degree in Life Sciences or associated fields with National Eligibility Test qualification, with a minimum of 60% marks or equivalent grade. Research experience and practical knowledge of working with laboratory rodent models is required. Knowledge of basic molecular biology techniques including PCR is required.
Clinical Regulatory Writing team provides expert communications leadership to drug projects and authors strategically important clinical-regulatory documents that are label focused and align with project strategies, regulatory requirements, and communications best-practices.
The successful candidate is expected to work on chickpea root nodule symbiosis, its transcriptomics and understanding the molecular mechanism behind plant immunity during root nodule symbiosis.
Candidates having M.Sc. or an equivalent qualification in Biotechnology, Bioinformatics or allied Life Science subjects with a minimum of 60% marks or an equivalent grade point are eligible to apply.
Switchable tandem CAR-T cells targeting tMUC1 and ROR1 for breast cancer immunotherapy. MSc Life Sciences with at least 60% marks in final exam and 3 years research experience or PhD in life sciences or MBBS with 3 years research experience or MD.
Performing Pharmacokinetic and statistical analysis, synthesizing research findings, and drafting scientific publications. Preferably with a minimum of 1 year of laboratory experience.