M.Pharm

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.

Ph.D degree in relevant field and first class or equivalent at either Bachelors or Masters level in the relevant branch. AND Minimum of 10 years of experience in teaching, research, industry out of which at least 3 years shall be at a post equivalent to that of an Associate Professor.

handle R&D projects independently in the areas of epidemiology, big data analytics, drug/ target/ biomarker discovery, preclinical and clinical evaluation of medical devices, IVDs, therapies, vaccines, field feasibility studies of the novel interventions, and experience/ exposure to regulatory aspects of health technologies, IP protection, Technology transfer. Health policy development and implementation. MD, MS or equivalent degree recognised by MCI, NMC OR MBBS or equivalent degree recognized by MCI, NMC, with MPH from a recognised university OR M.Sc or MBBS or equivalent degree, recognised by MCI, NMC, with Ph.D. from a recognised University.

Analytical method development, stability samples analysis and impurities identification by using instruments like HPLC, GC, LC-MS, and other analytical techniques.

Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.

Compile appendices to clinical study reports in compliance with appropriate regulatory requirements, with support of the project lead and lead medical writer. Work with internal or external Clinical and or Project Leadership functions to ensure that appendix documentation is complete and complies with the relevant guidelines.

Support the Quality vision and mission for Amgen India aligned with Amgen’s mission to serve patients. Support Amgen India Quality Team Lead in the development and implementation of a multi-year Quality technological plan aligned with Amgens standards and overall strategic imperatives.

PhD, MD, MS, MDS in Biochemistry, Biotechnology or an equivalent degree. OR Having 3 years of research, teaching, and design and development experience after MVSc, M.Pharm, ME, M.Tech with atleast one research paper in Science Citation Indexed Journal. 

Development of a nanostructured graphene oxide, polydopamine coated PDMS nano-biosensor monitoring GPC1 for the early diagnosis of pancreatic cancer.