
Siriporn Tanomchart
I have an experience in Clinical Research Field more tha 10 years. The current position in quintiles is Clinical... | Thailand
*50 free lookup(s) per month.
No credit card required.
Siriporn Tanomchart’s Emails si****@qu****.com
Siriporn Tanomchart’s Phone Numbers No phone number available.
Social Media
Siriporn Tanomchart’s Location Thailand
Siriporn Tanomchart’s Expertise I have an experience in Clinical Research Field more tha 10 years. The current position in quintiles is Clinical Project Manager and Clinical Research Manager. Job responsibilities 1. Study planning activities • Site Identification: perform country and site feasibility and summarize the information in a country • Investigator Contracting :Create and negotiate the Clinical Trial Agreement with the investigator, Forcast and accurate the trial budget. 2. Site start up activities • Create recruitment and study plan, including key timeline and monitoring frequency, communicate to local team and/or Global Team. • Prepare the country specific ICF, if applicable, a pharmacogenomic country specific ICF. • Ensure that the central IEC/IRB is provided a complete approval of all related required documents, including the composition of IEC/IRB. • Ensure the local RA approval and import/export permit license are obtain. Vendor and partner start-up • Perform UAT on trial related external systems and related manuals (such as IVRS) if applicable • Verify that IVRS is operational for the country • Verify that all predefined specifications are met in terms of functionality, reporting & interaction with other vendors • If applicable, identify local vendors, create and negotiate agreement with these vendors • Ensure that country-specific requirements for sample handling can be met and that the CRAs are properly trained in these requirements 3. Study execution activities • Implement an track recruitment strategies • Co-ordinate monitoring and ensure the monitoring frequency • Review the monitoring visit report • Accompany CRA • Track costs at country level 4. Study closure activities • Ensure that the IEC/IRB and regulatory authorities are notified of country and global trail completion and provide with the required document. •• Reconcile country budget
Siriporn Tanomchart’s Current Industry Iqvia
Siriporn
Tanomchart’s Prior Industry
Novartis
|
Roche Diagnosis
|
Quintiles
|
Iqvia
Not the Siriporn Tanomchart you were looking for?
Find accurate emails & phone numbers for over 700M professionals.
Work Experience

Iqvia
Clinical Research Manager
Wed Oct 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Quintiles
Clinical Project Manager
Sun Mar 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Sep 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Quintiles
Senior Clinical Research Associate
Sat Mar 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Feb 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)
Quintiles
Clinical Research Associate
Tue Mar 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Feb 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time)
Roche Diagnosis
Product Specialist
Sun Feb 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Mar 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis
Clinical Research Associate
Sun Dec 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time)