BAMS

D.Pharm or Master of Science in Medical Microbiology, Microbiology, Biotechnology, Biomedical Sciences ; with Doctor of Philosophy in Medical Microbiology, Microbiology, Biotechnology, Biomedical Sciences.

BHMS, BAMS, BUMS, BDS, B.Sc. Life science, M.Sc Life Science, B.Pharma., D. Pharma. and Diploma in Clinical Research. Preference will be given to the candidates having relevant experience in Clinical Research.

BHMS, BAMS, BUMS, BDS, B.Sc Life science, M.Sc Life Science, B.Pharma, D. Pharma and Diploma in Clinical Research. Preference will be given to the candidates having relevant experience in Clinical Research

Bachelors degree in Pharmacy, Bachelors of Ayurvedic medicine and surgery along with Post Graduate Diploma, Degree in Hospital Administration Management from recognised University.

qualification experience and should possess minimum M.Sc / B.Tech/ BE /MCA / MPH /B.Pharm/BAMS/ BSMS/ MD in AYUSH or equivalent qualifications in relevant subject. ; Post-graduates in Life Sciences, Sociology, MPH, Statistics, Social Work, Pharmacy, Nursing, Dentistry, Physiotherapy, equivalent qualifications

M.Pharma, MPT, MSc Nursing in Life Sciences or Equivalent. Or Graduate in Life Sciences BAMS, BHMS, Bsc Nursing, BPT or Equivalent from recognized University with three years of experience recognized University 

Postgraduate, Graduate degree in Science Eg. B.Pharm, Life Science, B.Sc., Biotech, Zoology, Botany, etc. with Diploma in Clinical Research is mandatory. One year experience in clinical trial monitoring is desirable.

Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable

Masters degree, diploma, life sciences, pharmacy, public health, healthcare or other related discipline with minimum 2 years of relevant clinical trial monitoring experience.