BDS

Post graduate degree in Life Science. OR Graduate, Post Graduate Degree In professional course e.g., M.Sc. Pharmacology, M.Pharm, MBBS,BDS selected through a process described through any one of the following Scholars who are selected through National Eligibility Test- CSIR-USG, NET including lectureship (Assistant Professorship) and GATE, GPAT.

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.

As the project is in its ending phase most of labwork is completed. Hence, Good manuscript writing skills and computer knowledge with knowledge of statistical analysis is required.

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

BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

Pharm.D, MPharm, BDS, MPH, MSc Biostatistics, MSc Clinical Research, MSc Nursing Or MSc Life Science, BTech Biotechnology with Post graduate Diploma in Clinical Research

Master degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice, and Clinical Research. OR Pharm.D, MBBS, BDS from a recognised university, Institute. 

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