Bangalore

Dual functional COX-2 inhibiting and antimicrobial NSAID-peptidomimetic conjugates as novel therapy to tackle septic infections. Ph.D, MD, MS, MDS or equivalent degree OR three years of research, teaching, design and development after MVSc, M.Pharm, M.E, M.Tech with at least tree research papers in high impact Journals. Candidates having research experience in organic synthesis, peptide synthesis, purification and characterization will be preferred.

Develop strategy to configure, distribute, and collect, and review and approve, high quality country specific and or site specific documents or essential regulatory documents and any updated or amended regulatory documentation.

As an Associate Global Scientific Advisor, you will Provide timely, accurate and credible scientific and medical input for a variety of projects pertaining to scientific communication around Novo Nordisk’s products. Collaborate closely and communicate effectively with various cross-functional stakeholders including colleagues from the US affiliate, global medical affairs, and other functional areas. Engage in dialogue with Key Opinion Leaders (KOLs) in different settings with focus on medical and scientific information. Prepare presentations for Novo Nordisk standalone events and international medical congresses.

First class post graduate degree including integrated PG degrees. Second class postgraduate degree including integrated PG degrees with PhD. Basic computer operating skills. This project is based in the neonatal intensive care unit. It recruits neonates, later preterm and term who are at risk of acute kidney injury and monitors them using a near-infrared spectroscopy device

The ideal candidate should be proficient in working with mouse brain, mammalian and stem cell culture, as well as basic and advanced molecular biology techniques such as cloning, transfection and epigenetic analysis. Additional skills include confocal, fluorescent microscopy. Masters degree in Science from a recognised university

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

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

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.