Total des années d'expérience: 14 Années, 7 Mois
mai 2013
A À présent
medical writer
à self-employed
Lieu :
Koweït - Al Farawaniyah
medical writing, online protocol formulation and review
juillet 2012
A mai 2013
Clinical Research associte
à Ananthapuri Hospitals and Research Institute
Lieu :
Inde
Implementation of projects and clinical trials, project management, checking their compatibility with ICH-GCP and Schedule-Y guldelines, training Clinical Research Coordinators, verification of Source douments, leading Research coordinator team etc.
août 2011
A juillet 2012
Clinical Research Coordinator
à Ananthapuri Hospitals and Research Institute
Lieu :
Inde
• Patient counseling and recruitment to clinical trials
• Site source document verification and monitoring
• Communicating with Project Manager, Principal Investigator, Subjects & Ethics committee
• Negotiating with Contract Research Organisation, Pharmaceutical Companies and Sponsors on behalf of the Principal Investigator.
• Know and follow the study protocol
• Maximize trial subject protection and data quality
• Maintain good trial files and archives
• Meticulously document product accountability
• Ensure timely & efficient safety reporting
• Check patient visit
• Filling up e-CRF (e- Case Report Form) and IVRS ( Interactive Voice Response System) processing
• Cooperating for auditing and monitoring
• Ensuring that the work done by Clinical Research Coordinator is up to the mark
• Check overall safety, quality and efficacy- compliance to ICH-GCP and Schedule Y guidelines.
• Site source document verification and monitoring
• Communicating with Project Manager, Principal Investigator, Subjects & Ethics committee
• Negotiating with Contract Research Organisation, Pharmaceutical Companies and Sponsors on behalf of the Principal Investigator.
• Know and follow the study protocol
• Maximize trial subject protection and data quality
• Maintain good trial files and archives
• Meticulously document product accountability
• Ensure timely & efficient safety reporting
• Check patient visit
• Filling up e-CRF (e- Case Report Form) and IVRS ( Interactive Voice Response System) processing
• Cooperating for auditing and monitoring
• Ensuring that the work done by Clinical Research Coordinator is up to the mark
• Check overall safety, quality and efficacy- compliance to ICH-GCP and Schedule Y guidelines.
novembre 2010
A août 2011
Clinical Research Coordinator
à PRS Hospital
Lieu :
Inde
• Patient counseling and recruitment to clinical trials
• Communicating with Project Manager, Principal Investigator, Subjects & Ethics committee
• Know and follow the study protocol
• Maximize trial subject protection and data quality
• Maintain good trial files and archives
• Meticulously document product accountability
• Ensure timely & efficient safety reporting
• Check patient visit
• Filling up e-CRF (e- Case Report Form) and IVRS ( Interactive Voice Response System) processing
• Cooperating for auditing and monitoring
• Check overall safety, quality and efficacy- compliance to ICH-GCP and Schedule Y guidelines.
• Communicating with Project Manager, Principal Investigator, Subjects & Ethics committee
• Know and follow the study protocol
• Maximize trial subject protection and data quality
• Maintain good trial files and archives
• Meticulously document product accountability
• Ensure timely & efficient safety reporting
• Check patient visit
• Filling up e-CRF (e- Case Report Form) and IVRS ( Interactive Voice Response System) processing
• Cooperating for auditing and monitoring
• Check overall safety, quality and efficacy- compliance to ICH-GCP and Schedule Y guidelines.
juillet 2009
A septembre 2010
Resident Siddha Medical Officer and Research Associate
à Santhigiri Ayurveda and Siddha Hospital and Research Centre
Lieu :
Inde - Delhi
• As a Siddha medical practitioner, treating patients as per Siddha principles and teaching them the Siddha way of life.
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