CDSA

Master’s degree in any field preferably in science, with 6 years of post- qualification experience in clinical data management/ clinical research/operations/ MIS/ data analysis/ IT/ computer science/ healthcare field

Post graduate degree in a Science or health related discipline with at least 15 years of work experience in clinical project management & monitoring and / or drug development

Bachelors in Life Science / Pharma. India Regulatory Science Course Development Support under Clinical Development Services Agency, CDSA center

Bachelors in Life Sciences with relevant clinical trial monitoring or clinical trial/study coordinator, or clinical trial/study associate experience. Masters degree/ diploma, life sciences, pharmacy, public health, healthcare

Postgraduate degree in Science/ Pharmacology/ Life Sciences/ Regulatory Science/ Public Health from a recognised University with atleast 6 years of relevant work experience

Postgraduate degree in Science / Pharmacology / Life Sciences / Regulatory Science/ Public Health from a recognised University with atleast 6 years of relevant work experience.

Masters Degree or PG Diploma or PhD in Life Sciences / Biomedical Sciences / Pharmacy / Public Health / Clinical Research with at least five years of experience in clinical project management and/or clinical trial/ study monitoring.

B.Pharm, Pharm.D or equivalent with two years post-qualification experience in clinical project management and/or clinical trial/ study monitoring in a recognised organisation / institute

Masters in any branch of Life Sciences from a recognized university. Candidate should have experience in gene cloning, protein expression and purification along with other microbiology, biochemistry and molecular biology techniques.  Translational Health Science and Technology Institute THSTI