Faculty & Staff
Freeda Xavier
1. M.Sc. - Clinical Research & Regulatory Affairs Sikkim Manipal University 2. B.Sc. - Microbiology Bangalore University
Program Manager
Languages
English, Hindi, Kannada, Tamil
- Overview
- Projects
- Publications
- Other Contributions
Contact : freeda@sjri.res.in
Experience
Program Manager
St. John's Research Institute
Senior Study Coordinator - Work with investigators on proposals with application and budgets for various granting agencies (UKMRC, NIH etc)
St. John's Research Institute
2009 onwards
Bangalore, India
Senior Study Coordinator - Conduct onsite visits for initiation, monitoring & for-cause visit, training of monitors, review the monitoring findings/action plan & resolution for the activities reported
St. John's Research Institute
2002 onwards (18 years)
Bangalore, India
Senior Study Coordinator - Coordinate multicentre clinical trials, registries, observational studies and translation research in acute coronary syndromes
St. John's Research Institute
2001 onwards (19 years)
Bangalore, India
Senior Study Coordinator - Procedures required for different regulatory requirements (study approvals, import license, annual reports, compensation requirement, sugam portal, CTRI, etc), SOP writing
St. John's Research Institute
2001 onwards (19 years)
Bangalore, India
Areas of interest
Coordinate Multicentric Clinical Trials; Registries & Observational Studies in Acute Coronary Syndromes; Training & Monitoring of Clinical Research
Program Manager
St. John's Research Institute
Senior Study Coordinator - Work with investigators on proposals with application and budgets for various granting agencies (UKMRC, NIH etc)
St. John's Research Institute
2009 onwards
Bangalore, India
Senior Study Coordinator - Conduct onsite visits for initiation, monitoring & for-cause visit, training of monitors, review the monitoring findings/action plan & resolution for the activities reported
St. John's Research Institute
2002 onwards (18 years)
Bangalore, India
Senior Study Coordinator - Coordinate multicentre clinical trials, registries, observational studies and translation research in acute coronary syndromes
St. John's Research Institute
2001 onwards (19 years)
Bangalore, India
Senior Study Coordinator - Procedures required for different regulatory requirements (study approvals, import license, annual reports, compensation requirement, sugam portal, CTRI, etc), SOP writing
St. John's Research Institute
2001 onwards (19 years)
Bangalore, India
Coordinate Multicentric Clinical Trials; Registries & Observational Studies in Acute Coronary Syndromes; Training & Monitoring of Clinical Research
No groups and associations specified.
| S.I. No | Project Title | Project Lead | Year of Initiation | Status |
|---|---|---|---|---|
| 1 | POISE-3 - Peri-Operative ISchemic Evaluation-3 | Dr. Denis Xavier | 2018 | ongoing |
| 2 | ACHIEVE -Aldosterone bloCkade for Health Improvement EValuation in End-stage renal disease | Dr Denis Xavier | 2019 | completed |
| 3 | ACT Study - Anti-Coronavirus Therapies (ACT) to prevent progression of COVID-19: Randomized trials | PI: Dr. Denis Xavier, Co-I: Dr. Prem Pais / Dr.Atiya Faruqui/ Dr. Bhuvana K B | 2020 | completed |
No publications details available.
No Others Contributions details available.