Responsibilities :
- Review protocol and provide suggestions
- Respond to queries / clarifications from EC / IRBs
- Answer medical questions from sites or project team
- Respond to queries from sites with regard to protocol
- Attend drug safety meetings / external meetings
- Patient eligibility review
- Review AE / SAEs
- Protocol training to site staff, CRAs etc
- Attend, participate / present in investigator meetings
Qualification : MBBS / MD qualification
Eligibility :
3 year+ of clinical trial experienceFamiliar with clinical trials operationsGood English communication skillsProficiency in using Microsoft officeSkills Required
Mbbs, Protocols, Drug Safety, Trainings, Investigations