JOB DETAILS

One of our clients, a reputed company in clinical research, is looking out for a Clinical Research Associate for their office based in Mumbai. The job responsibilities are as follows:


1. Act as monitor of specific sites on a clinical study, under supervision, as appropriate. 

2. Facilitate preparation and collection of site level documents.

3. Participate in trial site training activities, as assigned. 

4. Perform monitoring visits according to monitoring plan, as assigned, including source document verification.

5. Facilitate site drug supply management. 

6. Co-ordinate site level updates of technical systems (ClinAdmin, EDC).

7. Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc). 

8. Demonstrate and apply GCP and ICH requirements.

9. Prepare study monitoring reports under supervision, as appropriate. 

9.Assist with data que...