Randy Corley

Randy Corley

2510 Burningtree Dr SE, Decatur, AL 35603

07/17/2023

To Whom It May Concern:

I have over 25 years of experience in clinical research at the Sponsor, CRO, and Site level, including Director level positions, and I believe I would be an excellent fit with your organization. 

Until very recently, I served as the Director of Clinical Quality and Compliance for Imago BioSciences, a small biotech company.  I was instrumental in establishing and maintaining the audit schedule and conducting both investigator site and vendor audits. I also oversaw the implementation of GCP-related SOPs and related training.  Imago was recently purchased by Merck, I have come to the end of my retention period, and my position has been absorbed by Merck.  

Previously, I worked privately as a consultant for 18 years, performing internal and external GCP audits, drafting SOP’s, Work Instructions, staff development and training, etc. for CROs, Pharma, and investigative sites.  I have served as the Director of Quality Assurance for a trial management organization, giving me the opportunity to internally audit clinical studies in all phases in a direct and contract capacity. I have also managed budgets and contracts for Phase I-IV trials as well as drafted, negotiated and implemented NDAs, CTAs and research agreements of all types for both the public and private sectors.  

I would love to discuss your organization and your quality assurance situation with you.  Please feel free to contact me via phone, email, or LinkedIn.  I look forward to hearing from you soon.

Kind Regards,

Randy Corley

I have over 25 years of experience in clinical research at the Sponsor, CRO, and Site level, including Director level positions, and I believe I would be an excellent fit with your organization. 

Until very recently, I served as the Director of Clinical Quality and Compliance for Imago BioSciences, a small biotech company.  I was instrumental in establishing and maintaining the audit schedule and conducting both investigator site and vendor audits. I also oversaw the implementation of GCP-related SOPs and related training.  Imago was recently purchased by Merck, I have come to the end of my retention period, and my position has been absorbed by Merck.  

Previously, I worked privately as a consultant for 18 years, performing internal and external GCP audits, drafting SOP’s, Work Instructions, staff development and training, etc. for CROs, Pharma, and investigative sites.  I have served as the Director of Quality Assurance for a trial management organization, giving me the opportunity to internally audit clinical studies in all phases in a direct and contract capacity. I have also managed budgets and contracts for Phase I-IV trials as well as drafted, negotiated and implemented NDAs, CTAs and research agreements of all types for both the public and private sectors.

I have a Bachelor of Science degree from Excelsior College. I also have an Associate of Science degree in Business Administration.