Location- Bengaluru – IND
Basic Qualifications
- Knowledge of clinical research methodology, industry regulations and Good Clinical Practice guidelines related to human research.
- Aware of professional/clinical trial industry standards, in particular excellent knowledge of ICH GCP required.
- Expected to work independently, as well as in a team environment.
- Good organizational and administrative abilities
- Familiarity with MS Office and various business software
- Preferred: 0–2-year work experience in job areas such as:
- Clinical trial coordinator at site
- Clinical data management
- Pharmacovigilance
- Records management
