Alan Ashok Email & Phone Number | Being Study Start Up Associate or Regulatory document/ CDP reviewer, I am involved in review of essential documents including ethics/regulatory submission packages and site level critical documents and provides approval for site activation to commence the clinical trial at study site. Regulaory document review involves Verification of CA and EC approval for all study specific documents are in place, prior to the start of the study. Deliver Quality review of essential document packages adhering to requirements and guidelines referenced in ICH GCP Guidelines, DMID Regulatory File Document Guidelines, 45 CFR 46, 21 CFR 50 and 21 CFR 312

Alan Ashok

Being Study Start Up Associate or Regulatory document/ CDP reviewer, I am involved in review of esse...
Bengaluru, Karnataka, India

*50 free lookup(s) per month.

Alan Ashok’s Email aashok@iconplc.com

Alan Ashok’s Phone Numbers

Get ALAN’s Phone Number (For Free)

Social Media

Alan Ashok’s Location Bengaluru, Karnataka, India

Alan Ashok’s Current Industry

Alan Ashok’s Prior Industry Regional Cancer Centre Trivandrum | Kims Corporate Relation

Find accurate emails & phone numbers for over 700M professionals.

Senior Study Start Up Associate

Present

Clinical Research Coordinator

2009-03-01 00:00:00 - 2010-04-01 00:00:00

Clinical Research Coordinator

2008-02-01 00:00:00 - 2009-03-01 00:00:00

No Skills Available

No Languages Available

Alan Ashok is a Being Study Start Up Associate or Regulatory document/ CDP reviewer, I am involved in review of essential documents including ethics/regulatory submission packages and site level critical documents and provides approval for site activation to commence the clinical trial at study site. Regulaory document review involves Verification of CA and EC approval for all study specific documents are in place, prior to the start of the study. Deliver Quality review of essential document packages adhering to requirements and guidelines referenced in ICH GCP Guidelines, DMID Regulatory File Document Guidelines, 45 CFR 46, 21 CFR 50 and 21 CFR 312