Life Sciences

M.Sc. in Life Science /Nursing/ Biotechnology/ Microbiology /M. Pharma or equivalent. Candidate should have at least 6 year experience with Clinical Research Projects in academic setting and proficiency in English and Hindi language.

Master degree in Natural / Life Science form recognized university. Candidate with at least 2 years experience in Molecular / Cell Biology, sanger analysis & NGS Analysis will be preferred.

The candidate must hold an M.Sc. Botany, Biotechnology, Microbiology, Life Science, Applied Microbiology, biochemistry with first division in undergraduate and post graduate examination.

MTech in any area of Life Sciences, Biotechnology, MSc degree in any allied area of Life Sciences, Biotechnology, BTech, BPharm, BE (4-years degree programme) in any allied area of Life Sciences/Biotechnology, BVSc, MBBS, with minimum 60% marks.

Masters degree in Biotechnology/Biochemistry/Microbiology Bioinformatics/ Biotechnology/ Life science/Biomedical Sciences/Bio-Engineering passed with minimum 55% marks.

Responsible for safety monitoring and evaluation of assigned GSK products. Conduct safety monitoring and evaluation for assigned products, including signal detection and risk assessment.

Bachelors degree in Medical, Mechanical, Life Science or other healthcare related major. Works independently with general supervision on larger, moderately complex projects / assignments.

Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis

Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives. Prior experience with Data Management.