Cara Willoughby Email & Phone Number | • 24 years pharmaceutical industry experience in clinical trial planning and reporting, interpretation and application of global regulations for clinical trials, medical writing and preparation of marketing applications (regulatory submissions), and the development of new technology solutions. • 4 years leading/influencing the development of clinical trial and healthcare data interchange standards, particularly those for clinical trial protocols and regulatory submissions. • 12 years supervisory experience, >21 years of experience leading cross-functional teams • Strengths in strategic planning and design for Clinical Programs and Trials, process improvement, connecting people and ideas, written/oral communication, strategic influence, vision-setting, creative/abstract thinking, and meeting facilitation. Specialties: clinical development processes, drug development processes, structured authoring, content management, clinical interchange standards development organizations (CDISC, HL7), regulatory documents, next-generation authoring tools, clinical operations informatics

Cara Willoughby

• 24 years pharmaceutical industry experience in clinical trial planning and reporting, interpretati...
Chapel Hill, North Carolina, United States

*50 free lookup(s) per month.

Cara Willoughby’s Phone Numbers

Get CARA’s Phone Number (For Free)

Social Media

Cara Willoughby’s Location Chapel Hill, North Carolina, United States

Cara Willoughby’s Current Industry Iqvia

Cara Willoughby’s Prior Industry Quintiles | Eli Lilly | Cdisc

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

Senior Director, Design Analytics

2019-03-01 00:00:00 - Present

Director, Infosario Design Delivery Lead, Center for Integrated Drug Development

2012-01-01 00:00:00 - 2013-06-01 00:00:00

Informatics Consultant

2007-06-01 00:00:00 - 2011-05-01 00:00:00

Protocol Representation Group Colead

2003-01-01 00:00:00 - 2007-01-01 00:00:00

No Skills Available

No Languages Available

Cara Willoughby is a • 24 years pharmaceutical industry experience in clinical trial planning and reporting, interpretation and application of global regulations for clinical trials, medical writing and preparation of marketing applications (regulatory submissions), and the development of new technology solutions. • 4 years leading/influencing the development of clinical trial and healthcare data interchange standards, particularly those for clinical trial protocols and regulatory submissions. • 12 years supervisory experience, >21 years of experience leading cross-functional teams • Strengths in strategic planning and design for Clinical Programs and Trials, process improvement, connecting people and ideas, written/oral communication, strategic influence, vision-setting, creative/abstract thinking, and meeting facilitation. Specialties: clinical development processes, drug development processes, structured authoring, content management, clinical interchange standards development organizations (CDISC, HL7), regulatory documents, next-generation authoring tools, clinical operations informatics