Biobanking Research Specimens at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, September 30, 2013
1:00 pm - 3:00 pm
ClinicalTrials.gov
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, January 30, 2014
1:00 pm - 3:30 pm
Investigator Responsibilities
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, February 03, 2014
11:00 am - 1:00 pm
Human Subjects Research at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, February 10, 2014
11:00 am - 1:00 pm
Research Data Integrity/Data Security
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, February 10, 2014
1:30 pm - 3:30 pm
Adverse Events
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, February 11, 2014
10:00 am - 12:00 pm
Informed Consent
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, February 17, 2014
12:00 pm - 2:00 pm
Study Documentation: Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, February 20, 2014
12:00 pm - 2:00 pm
Human Subjects Research at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, March 04, 2014
11:00 am - 1:00 pm
Research Data Integrity/Data Security
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, March 04, 2014
1:30 pm - 3:30 pm
Biobanking Research Specimens at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, March 20, 2014
10:00 am - 12:00 pm
Recruiting Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, March 24, 2014
10:00 am - 12:00 pm
Investigator Responsibilities
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, April 08, 2014
11:00 am - 1:00 pm
Informed Consent
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, April 10, 2014
1:30 pm - 3:30 pm
Adverse Events
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, April 16, 2014
2:00 pm - 4:00 pm
Study Documentation: Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, April 21, 2014
1:30 pm - 3:30 pm
Human Subjects Research at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, May 05, 2014
11:00 am - 1:00 pm
Research Data Integrity/Data Security
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, May 05, 2014
1:30 pm - 3:30 pm
Investigator Responsibilities
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, June 02, 2014
11:00 am - 1:00 pm
Human Subjects Research at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, June 04, 2014
11:30 am - 1:30 pm
Research Data Integrity/Data Security
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, June 04, 2014
2:00 pm - 4:00 pm
Recruiting Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, June 05, 2014
10:00 am - 12:00 pm
Biobanking Research Speciments at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, June 19, 2014
12:00 pm - 2:00 pm
Study Documentation Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, July 08, 2014
1:00 pm - 3:00 pm
Phyllis Kennel
ClinicalTrials.gov Introduction
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, July 22, 2014
2:00 pm - 4:00 pm
Lorna Dula
Study Documentation Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, September 09, 2014
1:00 pm - 3:00 pm
Phyllis Kennel
Human Subjects Research at Duke Overview
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, September 17, 2014
1:00 pm - 3:00 pm
Donna Hamel
Recruiting Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, September 22, 2014
11:00 am - 1:00 pm
Sabrena Mervin-Blake
Research Databse Design
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, October 07, 2014
12:00 pm - 2:00 pm
Sue Budinger, Jeff Hawley, Ceci Chamorro
Study Documentation Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, October 14, 2014
1:00 pm - 3:00 pm
Catee Mullen
Adverse Events
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Wednesday, October 15, 2014
2:00 pm - 4:00 pm
Terry Ainsworth
The Informed Consent Process
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, October 16, 2014
1:00 pm - 3:00 pm
Pat Bixby
Budget Development and Negotiation Training
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, November 03, 2014
9:00 am - 11:00 am
Lindsey Spangler
Human Subjects Research at Duke Overview
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, November 11, 2014
11:00 am - 1:00 pm
Donna Hamel
Biobanking Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, December 01, 2014
1:00 pm - 3:00 pm
Helena Ellis and Alexis Sharp
Study Documentation Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, December 09, 2014
11:00 am - 1:00 pm
Donna Hamel
Recruiting Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Monday, December 15, 2014
1:00 pm - 3:00 pm
Sabrena Mervin-Blake
Human Subjects Research at Duke Overview
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Thursday, December 18, 2014
1:00 pm - 3:00 pm
Catee Mullen
Human Subjects Research at Duke
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, January 06, 2015
10:00 am - 12:00 pm
Study Documentation Regulations and Best Practices
Sponsor(s):
Duke Office of Clinical Research (DOCR)
Tuesday, January 06, 2015
12:00 pm - 2:00 pm
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