Masters degree, diploma, life sciences, pharmacy, public health, healthcare or other related discipline with minimum 2 years of relevant clinical trial monitoring experience.
Responsible for processing of Individual Case Safety Reports ICSRs from various sources, Literature search and review, signal detection and management, tracking regulatory information, performing regulatory submissions and supporting preparation of aggregate and other study reports, as well as Medical and Product Dictionary Management activities, where applicable
MD, MS or equivalent degree recognized by MCI, NMC OR MBBS or equivalent degree recognized by MCI, NMC with MPH from a recognized University OR M.Sc. or MBBS or equivalent degree recognized by MCI, NMC with Ph.D. from a recognized University.
Masters degree in Chemistry or Biochemistry or Pharmacy or Pharmaceutical Chemistry or Pharmacology or Bacteriology or Medicine or Microbiology or Biotechnology from a recognised University or institute.
Post Graduate from any one among following branch with NET qualification. Zoology, Pharmacy, Industrial Biotechnology, Biotechnology, Chemistry, any relevant subject of life sciences. Natural Farming vs Conventional farming, Understanding the Translational Dynamics of Microbiome, Drug and Pesticide residues in Animal Products.
Collaborate with outsource parties to full fill laboratory requirement in timely manner. Previous experience in analytical method validation would be an added advantage.
Post Graduate degree in any of the subjects viz- Biochemistry or Chemistry or Anthropology or Sociology or Social Work or food and Nutrition or Economics with specialization in Health Economies or Psychology or Biology or Bio science or Entomology or Genetics or Medical Genetics or Immunology or Microbiology or Molecular biology or Pharmacology or Pharmacy or Toxicology
He, She will be expected to participate in project planning, recording and interpretation, evaluation of data, and communication of results. He, She will also be expected to acquire technical, lab management, and manuscript, grant writing skills; and participate in seminars, lectures, poster sessions and presentations at national meetings.
PhD in Pharmacy Pharmaceutics, Pharmaceutical Chemistry, Pharmacology with a first-class career throughout; Candidates with experience in Teaching, Industry, Research and GPAT qualification will be given preference.
Overall coordination and conduct of the project activities including analysis and report writing along with the study team. Candidate is required to coordinate with Institute, other Centers selected under this call for proposal and monitoring the work under of multicentric project and assist the Program officer in review of the data collected and preparation of reports and any other work assigned by Program Officer.