Colleen Canavan

Director, Clinical Drug Development and Operations

Colleen Canavan is a eficient expert, that works in Horizon Pharma Plc on the position of Director, Clinical Drug Development and Operations from 2015. This expert has earned professional experience in more than 13 positions at different companies. Colleen Canavan went to the Lewis University and got education there from 2013 to 2015. Chicago, Illinois is the area, where this person was known to live. Their email address and number can be accessed through this website on demand.
Name variants:
Coleen Canavan, Lena Canavan
Last updated Jul 05, 2024

Contact Information

Last Update
Jun 22, 2022
Email
cc**@horizonpharma.com, cc**@yahoo.com, cc**@palosheights.org
Location
Chicago, IL
Company
Horizon Pharma Plc

Workplace

Director, Clinical Drug Development and Operations

Work History

Director, Clinical Drug Development and Operations

Horizon Pharma plc is a biopharmaceutical company focused on improving patients' lives by identifying, developing, acquiring and commercializing differentiated and accessible medicines that ...
from Oct 2015

Director, Clinical Drug Development and Operations

75 Varick St, New York, NY 10013
from Oct 2015

Unit Admitting Associate

from Jun 2012

Consultant Program Management

Nov 2009 — Sep 2015

Aquatics, Teen and Adult Coordinator

Illinois
Aug 2008 — Jun 2012

Director of Clinical Research and Development

235 Pine Ave, Carlsbad, CA 92008
Sep 2007 — Nov 2009

Consultant Program Managment

Jan 2005 — Aug 2005

Consultant Program Managment

Jan 2003 — Sep 2007

Therapeutic Area Scientist and Clinical Research Manager

New York, NY
Jan 1999 — Dec 2003

Senior Clinical Research Manager

Jul 1998 — Jan 1999

Project Manager

201 east 4Th St, Cincinnati, OH 45202
May 1997 — Jul 1998

Clinical Research Associate

Illinois
Feb 1994 — May 1997

Microbiologist I

Chicago, IL
May 1993 — Feb 1994

Occupations

Executive
Director
Operations Manager

Skills

Clinical Research
Pharmaceutical Industry
Gcp
Clinical Trials
Clinical Development
Ctms
Cro
Clinical Monitoring
Drug Development
Oncology
Regulatory Affairs
Ich Gcp
Therapeutic Areas
Biotechnology
Edc
Protocol
Pharmacovigilance
Clinical Trial Management System
Good Clinical Practice
Lifesciences
Neurology
Sop
Data Management
Cardiology
Regulatory Submissions
Cro Management
Medical Devices
Infectious Diseases
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