Natthakarn Paokaew

FAQ About Natthakarn Paokaew

• What is Natthakarn Paokaew's address?

  Natthakarn Paokaew is located at
  IQVIA, 1 Trok Tambisa, Thailand

• What is Natthakarn Paokaew's job title?

  Natthakarn Paokaew is a
  Over 12.2 years of experience working in clinical research with over 6 years of experience as RA. Responsibilities : Management of activities associated with obtaining initial and amendment. : Management of central/country level submissions associated with ensuring Investigational Product (IP) and any other clinical trial supplies can be imported and where applicable,the LRAA is responsible for : Ensuring that IP labels are in adherence to country requirements and submitted where applicable. : Tracking the IP/ Lab kit submission/approval progress in Clinical Trials Management System (CTMS) :Providing consultancy to the client on any country specifics issues if requested by the Start-Up Lead (SUL), LM or CPM. : Supporting the Senior level Regulatory staff/Country Consultant in the maintenance of the accurate, up to date Country Knowledge Repository. : Attending internal and external project team meetings as determined by SUL, or CPM. : If applicable for the Country, submit expectable safety reports to RAs with relevant legislation and the project-specific contractual agreement. : Providing RA training / updated RA requirements to all clinical research associates or any required. Iqvia

• What industry does Natthakarn Paokaew currently work in?

  Natthakarn Paokaew currently works in the
  Iqvia

• What is Natthakarn Paokaew's area of expertise?

  Natthakarn Paokaew specializes in
  Over 12.2 years of experience working in clinical research with over 6 years of experience as RA. Responsibilities : Management of activities associated with obtaining initial and amendment. : Management of central/country level submissions associated with ensuring Investigational Product (IP) and any other clinical trial supplies can be imported and where applicable,the LRAA is responsible for : Ensuring that IP labels are in adherence to country requirements and submitted where applicable. : Tracking the IP/ Lab kit submission/approval progress in Clinical Trials Management System (CTMS) :Providing consultancy to the client on any country specifics issues if requested by the Start-Up Lead (SUL), LM or CPM. : Supporting the Senior level Regulatory staff/Country Consultant in the maintenance of the accurate, up to date Country Knowledge Repository. : Attending internal and external project team meetings as determined by SUL, or CPM. : If applicable for the Country, submit expectable safety reports to RAs with relevant legislation and the project-specific contractual agreement. : Providing RA training / updated RA requirements to all clinical research associates or any required.

• Which languages does Natthakarn Paokaew speak? 

  Natthakarn Paokaew speaks the following languages:
  No languages available.

• Which industries has Natthakarn Paokaew previously worked in?   

  Natthakarn Paokaew has prior experience in the following industries:
  No prior industries available.

• What is Natthakarn Paokaew’s work experience?  

  Natthakarn Paokaew has the following professional experience:
  Iqvia .

• How can I find Natthakarn Paokaew on LinkedIn?  

  You can view Natthakarn Paokaew’s
  LinkedIn profile at LinkedIn URL.

• What are Natthakarn Paokaew’s work email addresses?  

  Natthakarn Paokaew’s work email addresses are
  [email protected] .

• What company does Natthakarn Paokaew work for?  

  Natthakarn Paokaew works at
  Iqvia