Lorrie Mills
Sr. Clinical Research Coordinator at Medicis- Claim this Profile
Click to upgrade to our gold package
for the full feature experience.
Topline Score
Bio
Gail Garrison
Lorrie was an exceptional team member. She always prepared high quality work and had it complete before the deadlines. I appreciated her consistent quality contibutions and would be proud to recommend her to anyone seeking a reference.
Sharron Gargosky, PhD
Lorrie is an asset to any clinical research group. She is an extremely hard working, diligent, detail oriented coordinator. Her background provides a fundamental, foundational understanding of the medical basis of the trial and she has the ability to translate the protocol into a working document that the study staff will be able to actuate. She has a breadth of experience in all aspect of clinical trial execution, documentation, agreements, and logistics. Her positive nature and good interpersonal skills enable her to interact with internal and external vendors and clients with ease. A wonderful person to have on any team.
Gail Garrison
Lorrie was an exceptional team member. She always prepared high quality work and had it complete before the deadlines. I appreciated her consistent quality contibutions and would be proud to recommend her to anyone seeking a reference.
Sharron Gargosky, PhD
Lorrie is an asset to any clinical research group. She is an extremely hard working, diligent, detail oriented coordinator. Her background provides a fundamental, foundational understanding of the medical basis of the trial and she has the ability to translate the protocol into a working document that the study staff will be able to actuate. She has a breadth of experience in all aspect of clinical trial execution, documentation, agreements, and logistics. Her positive nature and good interpersonal skills enable her to interact with internal and external vendors and clients with ease. A wonderful person to have on any team.
Gail Garrison
Lorrie was an exceptional team member. She always prepared high quality work and had it complete before the deadlines. I appreciated her consistent quality contibutions and would be proud to recommend her to anyone seeking a reference.
Sharron Gargosky, PhD
Lorrie is an asset to any clinical research group. She is an extremely hard working, diligent, detail oriented coordinator. Her background provides a fundamental, foundational understanding of the medical basis of the trial and she has the ability to translate the protocol into a working document that the study staff will be able to actuate. She has a breadth of experience in all aspect of clinical trial execution, documentation, agreements, and logistics. Her positive nature and good interpersonal skills enable her to interact with internal and external vendors and clients with ease. A wonderful person to have on any team.
Gail Garrison
Lorrie was an exceptional team member. She always prepared high quality work and had it complete before the deadlines. I appreciated her consistent quality contibutions and would be proud to recommend her to anyone seeking a reference.
Sharron Gargosky, PhD
Lorrie is an asset to any clinical research group. She is an extremely hard working, diligent, detail oriented coordinator. Her background provides a fundamental, foundational understanding of the medical basis of the trial and she has the ability to translate the protocol into a working document that the study staff will be able to actuate. She has a breadth of experience in all aspect of clinical trial execution, documentation, agreements, and logistics. Her positive nature and good interpersonal skills enable her to interact with internal and external vendors and clients with ease. A wonderful person to have on any team.
Experience
-
Medicis
-
United States
-
Pharmaceutical Manufacturing
-
200 - 300 Employee
-
Sr. Clinical Research Coordinator
-
Mar 2005 - Present
Primary liaison between the pharmaceutical sponsor and the Institutional Review Board. Liaison between research facilities and Medicis Pharmaceutical. Development of Case Report Forms, and Regulatory Documents for upcoming research trials. Payment processing, inventory control, Medical supply ordering. Operate TrialWorks clinical study program to facilitate study data management. Maintain weekly subject enrollment logs for data management.
-
-
Sr Clinical Trial Coordinator
-
2005 - Present
-
-
-
-
CCRC
-
2004 - 2005
-
-
-
-
CCRC
-
Jan 1999 - Apr 2004
-
-
CCRC Radiant Research
-
1999 - 2004
-
-
Education
-
University of Phoenix
BSB/M, Busnisess Management -
Glendale Community College
Nursing Education