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Freeda Xavier

Program Manager

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English, Hindi, Kannada, Tamil
  • Overview
  • Projects
  • Publications
  • Other Contributions

Division / Project : Clinical Research and Training

Designation :

  • Program Manager

Contact :

  • freeda@sjri.res.in

Qualification/ Education

  • M.Sc. - Clinical Research & Regulatory Affairs
    Sikkim Manipal University
  • B.Sc. - Microbiology
    Bangalore University

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
4 PROGRESS - Policy and peeR mentor intervention proGrams on cardiovascular disease at work Sites in 3 South Asian countries PI: Dr. Denis Xavier, Co-I: Dr. Deepak Kamath, Dr. Padmini Devi 2014 completed
5 Apollo – A randomized controlled trial of aliskiren in the prevention of Major Cardiovascular events in elderly people Dr. Prem Pais, Dr. Denis Xavier 2012 completed
6 A randomized controlled trial of timing of Intervention (early versus delayed) in Acute Coronary Syndromes (TIMACS) Dr. Prem Pais, Dr. Denis Xavier 2009 completed
7 A comparative study between standard and high dose of clopidogrel in patients with unstable angina or non-ST segment elevation myocardial infarction managed with an early invasive strategy (CURRENT / OASIS-7) Dr.Prem Pais, Dr. Denis Xavier 2009 completed
8 An observational study to determine predisposing conditions & regional variations in Atrial Fibrillation/flutter (RELY AF Registry) Dr. Prem Pais, Dr. Denis Xavier 2009 completed
9 Heart Outcomes Prevention Evaluation - 3 Study (HOPE-3) Dr. Prem Pais, Dr. Denis Xavier 2009 completed
10 A randomized controlled trial of radial versus femoral Percutaneous Coronary Intervention Access in Unstable Angina or Myocardial Infarction (RIVAL) Dr. Prem Pais, Dr. Denis Xavier 2007 completed
11 A registry that examined the treatment patterns and outcome of Acute Coronary Syndrome patients with renal dysfunction (CREATE ACS Registry) Dr. Prem Pais, Dr. Denis Xavier 2007 completed
12 A trial to evaluate standard Vs low dose adjunctive IV Unfractionated Heparin (UFH) in patients undergoing Percutaneous Coronary Intervention (OASIS-8/ FUTURA) Dr. Prem Pais, Dr. Denis Xavier 2007 completed
13 To evaluate Reviparin and Glucose-Insulin-Potassium in Acute Myocardial Infarction (CREATE trial) Dr. Prem Pais, Dr. Denis Xavier 2007 completed
14 Oasis 5-RCT of Fondaparinux Vs enoxaparin in unstable / non –ST segment elevation MI Dr. Prem Pais, Dr. Denis Xavier 2005 completed
15 The International Polycap Study-3 (TIPS-3): Design, baseline characteristics and challenges in conduct Denis Xavier 2018 completed
16 Effect of fixed dose combinations of metoprolol and amlodipine in essential hypertension: MARS – A randomised controlled trial. Denis Xavier* 2010 completed
17 Bleeding during treatment with aspirin versus apixaban in patients with atrial fibrillation unsuitable for warfarin: the apixaban versus acetylsalicylic acid to prevent stroke in atrial fibrillation patients who have failed or are unsuitable for vitamin K antagonist treatment (AVERROES) trial 2010 completed
18 Effects of a polypill (Polycap) on risk factors in middle-aged individuals without cardiovascular disease (TIPS): a phase II, double-blind, randomised trial 2008 completed
19 Rationale, design, and organization of the PeriOperative ISchemic Evaluation (POISE) trial: a randomized controlled trial of metoprolol versus placebo in patients undergoing noncardiac surgery 2005 completed
20 MACE Registry Feasibility - Nationwide Network of Management of Acute Coronary Event Registries 1900 completed
21 Effects of fondaparinux on mortality and reinfarction in patients with acute ST-segment elevation myocardial infarction: the OASIS-6 randomized trial 2003 completed
22 Heart Rescue India Evaluation: Mixed methods study. To assess the effectiveness of a quality improvement program to improve access and care of acute cardiovascular disease 2016 ongoing
23 SPREAD Study: A randomized trial comparing post discharge interventions to standard care in Acute Coronary Syndrome patients 2014 completed
24 TIPS-K: The Second Indian Polycap Study. Sponsor Cadila. 2014 completed
25 POISE-2: A large international, placebo-controlled, factorial trial to assess the impact of clonidine and acetylsalicylic acid (ASA) in patients undergoing noncardiac surgery who are at risk of a perioperative cardiovascular event 2014 completed
26 VISION Study: A cohort study to predict risk in peri-operative ischemia 2011 completed

Polypill with or without Aspirin in Persons without Cardiovascular Disease

Groups and Associations Salim Yusuf, D.Phil. Philip Joseph, M.D., Antonio Dans, M.D., Peggy Gao, M.Sc., Koon Teo, Ph.D., Denis Xavier, M.D., Patricio López-Jaramillo,
The New England Journal of Medicine 2020
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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)

Groups and Associations 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
Am Heart J 2014
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No Others Contributions details available.