MD

Conduct medical review of all trial subjects in assigned clinical trials to ensure high-quality, consistent medical data. Ensure patient safety and adherence to protocols, Good Clinical Practice, ICH Guidelines, local regulations, and SOPs.

M.Sc., M Pharm. B.Sc. Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards. Initiates, implements and champions process improvement techniques.

Good understanding of medical affairs function. Understanding of local regulatory policy and industrys code of practice related to drug registration, pharmaceutical promotion and clinical research.

Doctoral degree in science / Engineering / Technology / Pharma / MD / MS from a recognized University or equivalent. 

Master / Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences / MVSc / Animal Sciences. Doctoral Degree in Science/ Pharma/MD/MS from a recognized University or equivalent

MSc in Microbiology / Biotechnology / Biomedical Sciences / Life Sciences with experience in Microbiology/ Biotechnology/ Biomedical Sciences/ Mycology Laboratory.

Master / Integrated Masters in Natural or Pharmaceutical Sciences / MVSc / Animal Sciences or Doctoral Degree in Science / Pharma / MD / MS from a recognized University or equivalent.

Ph.D, MD, MS, MDS in Botany / Chemistry / Pharmacology or equivalent degree or having 3 years research, training and design and Development experience.

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 one research paper in Science Citation Index Journal.