Seminar on Clinical Research for Cardiovascular Pharmaceuticals

Overview:

Understanding basic clinical research requires excellent people and project management skills, and very good scientific writing and organization skills. Also paramount is gathering necessary information to manage the statistical analysis and data management of all the many clinical studies. The clinical development plans must be laid by experienced leaders and project managers. The clinical plan includes the budgets and timeline necessary to properly research the drug and advance it through all the testing necessary to achieve approval by FDA. 

Why should you attend?

This seminar should be attended to ensure the proper compliance and development of traditional and new cardiovascular medications. Failure to attend could result in poorly managed clinical trials, wasted financial resources and liability based law suits. The development of well-designed clinical trials and rigorous monitoring is required. From the literature review to the last appendix a complete understanding of regulations pertaining to clinical research and monitoring a well-designed protocol is necessary. All project managers know that the critical path thru clinical research is extremely tightly regulated and fraught with pitfalls. 

Who Will Benefit:

• Clinical Research Associates
• Scientists
• Nurses
• Pharmacists
• Pharmacologists
• Doctors
• Medical Directors

Speaker:

Charlene M. Jett

President- 3R's Management Consulting and Therapeutics Inc 

Charlene M. Jett lives in Vandalia Illinois about 70 miles east of St. Louis. She is a scientist, clinical researcher, consultant, adventurer, volunteer, daughter of Charles W. and Sybel Harre. Charlene is well educated and has a  Master's of Science in Management (1990) from Lake Forest Graduate School of Management, Lake Forest Illinois, a  Master's of Science in Biology (1980) from Northeastern Illinois University, Chicago, Illinois and a Bachelor's of Science in Physiology (1972) from University of Illinois, Champaign-Urbana, Illinois.

Location: Washington, DC Date: May 26th & 27th, 2016 Time: 9:00 AM to 6:00 PM

Venue: Courtyard Arlington Crystal City/Reagan National Airport

Address: 2899 Jefferson Davis Highway Arlington, VA 22202 USA

Price: $1,295.00 (Seminar for One Delegate)

Register now and save $200. (Early Bird)

Until April 20, Early Bird Price: $1,295.00 from April 21 to May 24, Regular Price: $1,495.00

Quick Contact:

NetZealous DBA as GlobalCompliancePanel

Phone: 1-800-447-9407

Fax: 302-288-6884

Email: support@globalcompliancepanel.com      

Website: http://www.globalcompliancepanel.com/

Registration Link - http://bit.ly/clinical-research-Washington-DC