NEW! Cancer Research Career Development Course from the MCW Cancer Center

Clinical Trials: From Concept to Publication

 

This course will cover broad topics regarding clinical cancer trial design and development and is intended to increase the number of investigator-initiated trials at MCW and to improve the quality of proposed studies. The course is designed for clinicians who are new to cancer clinical research, junior faculty, and new faculty who wish to orient to MCW's clinical research systems. It is highly recommended for those applying for MCW Cancer Center pilot funds for clinical or translational research.

This offering is meant as a complete course of seven sessions, and we encourage participants to attend all sessions.  

Please register using the form below, and be sure to hit the green "Submit" button at the bottom. If you have any questions, contact Anne Mathias

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  List of Courses and Presenters

11/18/16
“Using Biostatistics for Effective Clinical Trial Design” 
Presented by James J. Dignam, PhDAssociate Professor, Biostatistics, Department of Public Health Sciences, University of Chicago and Deputy Group Statistician, NRG Oncology Cancer Center, 3rd Floor, Conference Room M

1/20/17
“Developing and Executing Persuasive and Relevant Clinical Research Ideas”  
Presented by Timothy Fenske, MD, MS; Stuart Wong, MD; Parameswaran Hari, MD, MS  Cancer Center, 3rd Floor, Conference Room M

2/17/17
“Understanding the CTO Protocol Development Process”  
Includes an overview of the Scientific Review Committee and the Data and Safety Monitoring Board, presented by James Thomas, MD, PhD; Ehab Atallah, MD; Betty Oleson, BSN, RN; Jennifer Bollmer, PhD  Center for Advanced Care, 1st Floor, Conference Room Q

3/17/17
“FDA and MCW Regulatory Requirements for Sponsor-Investigator Protocols" 
Includes annual reporting, serious adverse event reporting and responsibilities of sponsor investigator, presented by Marilyn Linde, CCRP; Becca Selle, CCRP; AnnMarie Eve; Kate Gaudreau  Cancer Center, 3rd Floor, Conference Room M

4/21/17
“Developing an Effective and Realistic Budget for Your Trial” 
Presented by Brenda Brito and Betty Oleson, BSN, RN Center for Advanced Care, 1st Floor, Conference Room Q

5/19/17
“Correlative Endpoints:  How and Why?” 
Presented by Hallgeir Rui, MD, PhD  Cancer Center, 3rd Floor, Conference Room M

6/16/17
"Interim Analyses in Clinical Trials" 
Presented by Aniko Szabo, PhD  Center for Advanced Care, 1st Floor, Conference Room Q

First Name   Last Name 

Credentials   Title 

Institution 

email   Phone 

My faculty mentor is 

I Plan to Attend: (Please check all that apply.)

11/18/16   “Using Biostatistics for Effective Clinical Trial Design” 

1/20/17     “Developing and Executing Persuasive and Relevant Clinical Research Ideas”  

2/17/17     “Understanding the CTO Protocol Development Process” 

3/17/17     “FDA and MCW Regulatory Requirements for Sponsor-Investigator Protocols” 

4/21/17     “Developing an Effective and Realistic Budget for Your Trial”

5/19/17     “Correlative Endpoints:  How and Why?”

6/16/17     "Interim Analyses in Clinical Trials" 

What are your reasons for participating in this course? (Please check all that apply.) 

I am new to clinical research and interested in designing / initiating clinical trials.

I am a clinical researcher who would like to improve my trial design.

I am new to MCW.

The course was suggested by my mentor.

I plan to apply for MCW Cancer Center pilot funds for clinical research.

Other  Please Explain 

Are there topics or issues that you would like to see covered in the course? 

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Page Updated 01/12/2017
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