Faculty & Staff
Preeti Girish
Clinical Research and Training
Languages
English, Hindi, Malayalam, Gujarati
- Overview
- Projects
- Publications
- Other Contributions
Division / Project : Clinical Research and Training
Designation :
- Senior study coordinator
Contact :
- preeti@sjri.res.in
Qualification/ Education
- 2010 - 2011; Distance-Based Certificate Program - Promoting Enhanced Research Capacity (PERC) for Global Health for International Study Coordinators
The University of Alabama School of Nursing, University of Alabama at Birmingham. Sponsored by the National Institutes of Health, Fogarty International Centre - 2007; PG Diploma in Clinical Research
ICRI, Bangalore - 2001; MSc - Environmental Science
Gujarat University, Gujarat - 1999; BSc - Biochemistry
Gujarat University, Gujarat
Experience
- Senior Study Co-ordinator: Experience in coordination of various activities related to large multicentre clinical trials and observational studies
St. John's Research Institute
2022-till date
Bangalore, India - Study Coordinator - Experience in coordination of various activities related to large multicentre clinical trials and observational studies for 13 years
St. John's Research Institute
2007 - 2022
Bangalore, India - Study Coordinator - Contributed to preparation of study specific documents such as informed consent, SOPs, manual of operations, regulatory documents, CRF, contract, CTRI registration, etc
St. John's Research Institute
2007 - 2022
Bangalore, India - Study Coordinator - Assisted investigators in study set up activities, institutional ethics committee submission, regulatory submissions, budget preparation, investigators meetings & training session
St. John's Research Institute
2007 - 2022
Bangalore, India - Study Coordinator - Vast experience in planning and conducting on-site monitoring visits for multicentre clinical trials
St. John's Research Institute
2007 - 2022
Bangalore, India
Areas of interest
Coordination of large Multicentre Clinical Trials and Observational Studies; CRA Training & Monitoring
- Senior Study Co-ordinator: Experience in coordination of various activities related to large multicentre clinical trials and observational studies
St. John's Research Institute
2022-till date
Bangalore, India - Study Coordinator - Experience in coordination of various activities related to large multicentre clinical trials and observational studies for 13 years
St. John's Research Institute
2007 - 2022
Bangalore, India - Study Coordinator - Contributed to preparation of study specific documents such as informed consent, SOPs, manual of operations, regulatory documents, CRF, contract, CTRI registration, etc
St. John's Research Institute
2007 - 2022
Bangalore, India - Study Coordinator - Assisted investigators in study set up activities, institutional ethics committee submission, regulatory submissions, budget preparation, investigators meetings & training session
St. John's Research Institute
2007 - 2022
Bangalore, India - Study Coordinator - Vast experience in planning and conducting on-site monitoring visits for multicentre clinical trials
St. John's Research Institute
2007 - 2022
Bangalore, India
Coordination of large Multicentre Clinical Trials and Observational Studies; CRA Training & Monitoring
No groups and associations specified.
Polypill with or without Aspirin in Persons without Cardiovascular Disease
Yusuf S, Joseph P, Dans A, Gao P, Teo K, Xavier D, López-Jaramillo P, Yusoff K, Santoso A, Gamra H, Talukder S, Christou C, Girish P, Yeates K, Xavier F, Dagenais G, Rocha C, McCready T, Tyrwhitt J, Bosch J, Pais P; International Polycap Study 3 Investigators Rationale and design of a randomized controlled trial evaluating community health worker-based interventions for the secondary prevention of acute coronary syndromes in India (SPREAD)
Kamath DY, Xavier D, Gupta R, Devereaux PJ, Sigamani A, Hussain T, Umesh S, Xavier F, Girish P, George N, Thomas T, Chidambaram N, Joshi R, Pais P, Yusuf S No Others Contributions details available.