Karnataka

Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies

The recruited candidate will perform majority of experiments proposed in the study, which includes preparation and characterization of nanoparticles, in vitro and in vivo safety and efficacy analysis etc. The Project Research Scientist-I will also take care of consumables ordering, storage and maintenance. The candidates with M.Sc., qualification shall enrol for Ph.D programme.

Postgraduate degree including the integrated PG degree in any branch of Life Sciences - Biological Sciences, Biotechnology, Biochemistry, Genetics.

Candidates with strong background in protein biochemistry, molecular biology and cell biology are encouraged to apply. Candidates are expected to have the ability to work independently, have good organizational skills, work in an interdisciplinary team, and manage multiple tasks. They will also be responsible for data documentation, validation and compilation, for preparation of manuscripts. Master degree in Life Sciences subjects or MVSc or Bachelors degree in engineering or technology

National Survey for Community Perspective Assessment and Preventive Strategies for Malaria Control in Selected Malaria Endemic States, India. Liaisoning with the state officials, private health facilities. Project implementation, data collection at study sites.

Ph.D and experience in Analytical Chemistry HPLC, HPTLC, MS, Flash Chromatography, in vitro studies involving mammalian cell lines, enzyme inhibition assays, antioxidant assay, Schrodingers platform, LIGPLOT, in vivo studies involving handling of transgenic mice, western blotting, qPCR, cloning, gene expression studies, Microbiology, Microscopy, Immunohistochemistry etc.

Performing medical writing tasks for trial and/or non-trial activities within clinical reporting including but not limited to preparation of Protocols, Clinical Trial Reports CTRs, Non-interventional study reports NSRs, Layperson Summary LPS, Investigator Brochure and Regulatory response documents. PhD, MSc, MPharm, PharmD

The educational qualifications remain the same as for the regular candidates. Qualifying in one of the national entrance tests like CSIR-UGC NET for JRF, UGC-NET for JRF, DBT JRF, ICMR JRF, GATE, and NBHM is desirable but not mandatory. Further, the candidate should have completed two years of full-time employment in the current organization after completion of degree. The candidates must be officially sponsored by their employing organizations and compulsorily fill in an online application form and submit the printed version, in duplicate, on or before 07th April 2025.

Good knowledge of triple quodrupole mass spectrometer platforms and demonstrated operational independence on these platforms. Experience in bioanalysis of small molecules is must to have and knowledge about other modalities such as biomarkers, cyclic peptides is preferred.