Faridabad

Masters degree diploma, life sciences, pharmacy, public health, healthcare or other related discipline with a minimum of 2 years of relevant clinical trial monitoring experience.

Will be responsible for overall administration of Ind-CEPI activities at THSTI. This will involve coordinating the construction and usage of shared infrastructure facilities at THSTI, leading regional networking and capacity building with LMIC’s and CEPI support from the Project Management Unit in oversight of the RFPs selected for funding etc

MSc / MTech in Life Sciences / Biotechnology / Molecular Biology / Biochemistry/ Bioinformatics / Genomics / Agriculture / Pharmacy or any other related subject, and National level JRF eligibility test, such as NET, GATE, etc., qualified.

MSc or Ph.D. in any branch of Life Sciences from a recognized university. Advance knowledge of virology, biochemistry, immunology and molecular biology related to recombinant protein expression, purification and characterization

Doctoral Degree in Life Science, Biotechnology and research experience in cell biology, molecular biology, and virology. Identification of the host proteins binding specifically to Chikungunya virus genomic RNA

Developing Repertoire of Orally Deliverable Phospholipid-Drug Conjugates for targeting Colorectal and Hepatocellular Carcinoma. MSc Biotechnology, Chemistry, Pharmacy, Pharmacology qualified with any National Level Test.

M.Pharma/ equivalent degree in any branch of Life Sciences; Investigating and translating genomic evidence for public health response to SARS- CoV-2

Post-Graduation degree, including the integrated PG degree, in any branch of Life Sciences from a recognized university with five years of post-qualification experience of working with mammalian expression, stable CHO cell line or mRNA vaccine platform and strong molecular biology experience.

Conduct site monitoring visits from initiation through closeout, ensuring trials are conducted in compliance with the study protocol, GCP guidelines, SOPs, and applicable regulatory requirements. Set up trial sites, ensuring that investigational products and essential trial supplies are delivered, stored, and documented appropriately.