Clinical Research Job Opportunity at SJRI | Apply Now
Looking for a clinical research job in Bangalore? St. John’s Research Institute (SJRI) is inviting applications for the position of Clinical Research Monitor under the TIPS-3 PHRI Study. This is an excellent opportunity for candidates with MBBS, BVSc, BDS, MPHW, or a postgraduate degree in clinical research who are seeking career growth in drug-based clinical trials. If you are exploring MBBS jobs in Bangalore or looking for rewarding BDS jobs in research, this role offers valuable hands-on clinical trial experience.
Job Details:
- Job Position: Clinical Research Monitor – TIPS-3 PHRI Study
- Project Name: TIPS-3 PHRI Study
- Number of Vacancy: One
- Location: Bangalore
- Salary: Rs. 50,000 per month
About the Institute:
St. John’s Research Institute is a premier medical research institution based in Bangalore, known for its excellence in public health and clinical research studies. The institute actively conducts drug-based clinical trials and contributes significantly to advancing healthcare research in India. If you are searching for sjri careers, this opportunity offers strong research exposure in a reputed institution.
Job Description:
This clinical research job is part of a Drug Based Clinical Trial under the TIPS-3 PHRI Study. The selected candidate will assist seniors in the ongoing clinical trial by carrying out coordination activities and supporting the monitoring process. The role includes undergoing training on monitoring processes, scheduling monitoring visits, conducting monitoring visits, and providing training to sites on GCP (Good Clinical Practice) and study activities. This opportunity is ideal for candidates looking for MBBS jobs in Bangalore, research-based BDS jobs, or professionals interested in strengthening their career in clinical trials.
Qualifications:
Preferred Qualifications:
- MBBS / BDS
- Graduate or Post Graduation with a Diploma in Clinical Research
Experience Required:
- 2 years of experience as a Site CRA
- Willingness to travel
Key Responsibilities:
The Clinical Research Monitor will be involved in the following phases and activities:
- Site Feasibility
- Initiation Visit
- Recruitment Phase
- Follow-up Phase
- Closeout Phase
- For Cause Visits
- Audit & Inspection
- Coordination activities in ongoing clinical trials
- Scheduling and conducting monitoring visits
- Providing training to sites on GCP and study activities
