We found the following information about Jason Jones at Wright Medical Technology, where this person has worked as a VP, Clinical Affairs since 2013. Jason's total work experience is over 26 years, during which time they had at least 13 jobs at different companies to develop professional skills. Jason studied at the University of Utah from 1994 to 2001. Jason received the following certifications: Certified Clinical Research Professional, Regulatory Affairs Certified (Rac (Us)), and Society of Clinical Research Associates. Jason Jones is experienced in English. Currently, Jason lives in Tiptonville, Tennessee. You can contact with Jason by searching for phone number or email address or find further info by requesting access to Jason's further details.
Name variants:
Jayson Jones,
Jay Jones
Last updated May 25, 2024
Contact Information
Last Update
Jul 14, 2022
Email
al**@gmail.com
Location
Tiptonville, TN
Company
Workplace
Colleagues
Work History
VP, Clinical Affairs
Arlington, TN
Responsible for clinical services on a global basis for biologics, extremities, and foot & ankle.
from Mar 2013
Vice President, Clinical Affairs
Arlington, TN
2013 — 2015
Immediate Past President
Provided guidance and direction to the organization by designing and implementing new clinical research education opportunities to our membership with a special emphasis in eLearning.
from Sep 2012
Global Vice President, Clinical Affairs
Memphis, TN
Responsible for all premarket, post market and investigator-initiated advanced surgical device clinical studies and data management activities in North America.
May 2011 — Feb 2013
Group Director, Clinical Affairs
Responsible for all premarket, post market and investigator-initiated advanced surgical device clinical studies and data management activities in North America. Created the business plan, o...
Mar 2009 — May 2011
Global Vice President / Group Director, Clinical Affairs
Cordova, TN
2009 — 2013
Associate Director, Research Program Management
Managed the $43M project development timelines associated with several pharma product pipelines.
Oct 2006 — Mar 2009
Clinical Project Manager
Managed all aspects of clinical studies, especially recruitment oversight, trial master file completion, providing study progress and status updates to Sponsors, etc.
2006 — 2006
Clinical Projects Manager
Managed the development and start-up of a complex multi-site IDE study for a novel carotid stent.
2004 — 2006
Clinical Affairs Manager
Was responsible for the day-to-day oversight of clinical affairs activities within the post market study division.
2001 — 2004
Education
1994 — 2001
1990 — 1993
Occupations
Executive
Vice President
Chairperson
Chief Executive
Skills
Clinical Trials
Medical Devices
Fda
Clinical Research
Clinical Development
Pharmaceutical Industry
Biotechnology
Gcp
Ctms
Healthcare
Orthopedics
Orthopedic
Cross Functional Team Leadership
Regulatory Affairs
Cardiology
Clinical Study Design
Strategic Planning
Cro
Leadership
Life Sciences
Process Improvement
Product Development
Quality Assurance
Research
Surgery
Program Management
Budgets
Data Management
Contract Negotiation
Lifesciences
Clinical Monitoring
Clinical
Hospitals
Iso 13485
Clinical Data Management
Biologics
Pharmaceuticals
Budgeting
Compliance
Clinical Trial Management
Writing
Powerpoint
Research Design
Foot Surgery
Report Writing
Quality Auditing
Mergers and Acquisitions
Peripheral Vascular
Dermatology
Joint Replacement
CTMS
Data Management
Budgeting
Forecasting
vendor outsourcing
building effective teams
strategic planning
employee development
regulatory compliance