Should possess minimum M.Sc / B.Tech / BE /MCA / MPH / B.Pharm/BAMS/ BSMS/ MD in AYUSH or equivalent qualifications in relevant subject with relevant experience (minimum 5 years) in managing any international/National registry, training in regulatory guidelines related to Biomedical and Health Research.
Pharmacy (B. Pharm), Life Sciences, or a related healthcare field OR Nursing (B.Sc. Nursing), Life Sciences, or a related healthcare field with 2 years relevant experience
First Class M.Pharm, MS (Pharm) Masters in Pharmacognosy or Bachelor of Ayurvedic Medicine and Surgery. PhD in Natural Product Chemistry, Life Sciences, Pharmaceutical Sciences or related disciplines.
Masters degree diploma, life sciences, pharmacy, public health, healthcare or other related discipline with a minimum of 2 years of relevant clinical trial monitoring experience.
1st class Post graduate Degree in Public Health, Epidemiology, Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacology from a recognized university with 3 years experience.
Professionals having proven competency and success in their area of specialization, with at least 1 years of post-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.
Bachelors degree in Pharmacy, Bachelors of Ayurvedic medicine and surgery along with Post Graduate Diploma, Degree in Hospital Administration Management from recognised University.
Conduct site monitoring visits from initiation through closeout, ensuring trials are conducted in compliance with the study protocol, GCP guidelines, SOPs, and applicable regulatory requirements. Set up trial sites, ensuring that investigational products and essential trial supplies are delivered, stored, and documented appropriately.