May enter data or assist in the creation of cases into the safety database in accordance with Sponsor, customer specific guidelines and Company standards if required.
Masters Degree / PG Diploma in Life Sciences / Biomedical Sciences / Pharmacy / Public Health / Clinical Research with experience in clinical project management and/or clinical trial/ study monitoring.
Doctorate in life sciences or biomedical sciences or Pharmacy or Clinical Sciences OR Masters degree in life sciences or biomedical sciences or pharmacy or public health or clinical 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
Masters degree, Ph.D in Public Health, Epidemiology, Life Sciences. OR Health Care Management, Health Administration after MBBS, BHMS, BDS or any other medical professional course in health Science.
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.
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.