[vc_row][vc_column][vc_single_image image=”2278″ alignment=”center” border_color=”grey” img_link_large=”” img_link_target=”_self” img_size=”medium”][vc_column_text disable_pattern=”true” align=”left” margin_bottom=”0″]In collaboration with the Centre for Support and Training in Analysis and Research (CSTAR) the HRB-TMRN will host two study days in January 2016 on Clinical Trial Design Biostatistics.
- UCC, 14th January 2016 – venue TBD
- UCD, 21th January 2016 – venue TBD
Overview:
This Study day is on Intermediate level biostatistics for clinical trials. The focus is on Trial Design, and will cover issues around defining and selecting endpoints, from a clinical, epidemiological and statistical point of view. We will then proceed to discussion and exercises on sample size calculations for clinical trials, with specific focus on composite endpoints, clustered designs, and on consideration of endpoints involving change over time. We conclude the day with discussion and exercises on randomisation, covering stratified, block, and adaptive procedures.
Registration will open shortly and places will be strictly limited.[/vc_column_text][vc_empty_space height=”32px”][vc_tweetmeme type=”horizontal”][vc_empty_space height=”32px”][vc_facebook type=”standard”][/vc_column][/vc_row]
