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Dewey Denham

Associate Director, Clinical Operations

Senior Director, Global Quality Control

Phoenix, Arizona Area

Section title

Dewey Denham's Work Experience

TAP Pharmaceuticals

Associate Director, Clinical Operations

2005 to 2008

Covance

Director, Clinical Operations

April 2012 to June 2013

Peoria, AZ

Purdue Pharma

Regional Manager, Western U.S.

February 2003 to August 2005

Dewey Denham's Education

Arizona State University

BS, Molecular Biology

1989 to 1992

Dewey Denham's Professional Skills Radar Chart

Based on our findings, Dewey Denham is ...

Easily distracted
Outgoing
Individualistic

What's on Dewey Denham's mind?

Based on our findings, Dewey Denham is ...

48% Left Brained
52% Right Brained

Dewey Denham's Estimated Salary Range

About Dewey Denham's Current Company

TAP Pharmaceuticals

Directly managed a staff of seven Clinical Operations managers and indirectly managed approximately 60 Clinical Operations staff. Directed operations for multiple functional areas, including Clinical Field Operations (monitoring) and Clinical Systems. Responsible for all financial aspects of Clinical Operations, including departmental budget and resource planning for approximately 150 staff.

Frequently Asked Questions about Dewey Denham

What company does Dewey Denham work for?

Dewey Denham works for TAP Pharmaceuticals


What is Dewey Denham's role at TAP Pharmaceuticals?

Dewey Denham is Associate Director, Clinical Operations


What is Dewey Denham's personal email address?

Dewey Denham's personal email address is d****[email protected]


What is Dewey Denham's business email address?

Dewey Denham's business email addresses are d****[email protected], and d****[email protected]


What is Dewey Denham's Phone Number?

Dewey Denham's phone (602) ***-*464


What industry does Dewey Denham work in?

Dewey Denham works in the Pharmaceuticals industry.


About Dewey Denham

đź“– Summary

Associate Director, Clinical Operations @ TAP Pharmaceuticals Directly managed a staff of seven Clinical Operations managers and indirectly managed approximately 60 Clinical Operations staff. Directed operations for multiple functional areas, including Clinical Field Operations (monitoring) and Clinical Systems. Responsible for all financial aspects of Clinical Operations, including departmental budget and resource planning for approximately 150 staff. From 2005 to 2008 (3 years) Director, Clinical Operations @ Covance Strategic responsibility to conduct clinical monitoring of investigative sites for clinical studies in North America. Global lead for directing achievement of corporate quality goals through creation and ongoing management of global metric reports. Develop strategies and lead initiatives to improve overall organizational efficiency. Provide leadership and guidance to Clinical Operations Managers responsible for managing the day-to-day site management activities. Responsible for directing Clinical Operations to execute on all assigned clinical trials based on clinical research policies and procedures to ensure global regulatory compliance. From April 2012 to June 2013 (1 year 3 months) Peoria, AZRegional Manager, Western U.S. @ Purdue Pharma Responsibility for the transition from an in-house to a regional monitoring program. Served as the Lead CRA Manager. Managed CRA organization for Western half of U.S (~ 20 CRAs). From February 2003 to August 2005 (2 years 7 months) Principal CRA @ Wyeth Pharmaceuticals Held supervisory/management responsibilities that involved conducting the performance review of new CRAs, assisting in the hiring of new CRAs, coordinating the training of new CRAs, implementing professional development/growth plans for new CRAs, and serving as the acting Assistant Director in the absence of supervisor. From April 1993 to January 2003 (9 years 10 months) Senior Director, Global Quality Control @ Covance * Lead the Global Quality Control team in the execution and continual evolution of the organizational quality control strategy Director, Global Quality Control @ Covance • Leadership role within the Global Quality Control team with primary accountability for management and oversight of all Quality Control activities relating to GCP compliance for functional departments (e.g. Global Clinical Trial Operations, Project Management, etc..) • Responsible for developing and delivering to the Quality Control Strategy • Responsible for the development and management of the Quality Control metrics systems across the assigned functions• Responsible for collaborating with functional leaders to drive compliance to quality objectives and improvements in quality metrics that demonstrate the business is operating in a quality state of control• Provide guidance to functional departments as to the quality status of the their business• Responsible for leading and managing a team of Quality Control Senior Managers, Associate Directors and other staff as identified by management• Assist the assigned functional organization with promotion of a proactive quality management culture Peoria, ArizonaAssociate Director, Global Quality Control @ Covance • Provide guidance to the GM as to the quality status of North America region and the actions required to support quality delivery.• Prepare an annual quality control plan with the respective operational leads based on prior client and Quality Assurance audits, regulatory inspections and the project specific operation plans.• Maintain, manage and co-ordinate the overall Quality Control (QC) plan for the region.• Ensure compliance with CAPAs, audit excellence, quality plan execution, QC metrics and quality training and communication as required.• Own and drive compliance to QC process and QC tools to ensure the integrity of metrics and performance.• Assist with promotion of a proactive quality culture. From June 2013 to September 2015 (2 years 4 months) Peoria, AZDirector, Site Management @ Takeda Pharmaceutical Company Ltd The Director of the Site Management department has overall strategic responsibility to conduct clinical monitoring of investigative sites and study management for clinical studies in the United States. Responsible for directing this organization to deliver world-class clinical trial monitoring and management; execute based on clinical research policies and procedures to ensure global regulatory compliance. The Director will provide leadership and guidance to Associate Directors and Senior Managers responsible for managing the day-to-day site management activities. From June 2008 to March 2012 (3 years 10 months)


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In a nutshell

Dewey Denham's Personality Type

Extraversion (E), Intuition (N), Thinking (T), Perceiving (P)

Average Tenure

3 year(s), 9 month(s)

Dewey Denham's Willingness to Change Jobs

Unlikely

Likely

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