UB's Clinical Research Office helps investigators and their staff to create, establish and manage research that advances our understanding of human health and behavior. The CRO and its staff members ...

Research into disease mechanisms and the development of disease diagnostics / therapeutics requires an understanding of clinical trial design including the ethical and regulatory requirements required ...

All clinical studies described above can be submitted ... The role of the sponsor in any stage of the study, including in study design, data analysis or manuscript preparation, must be acknowledged.

A career in clinical pharmacology — the study and use of drugs in humans — offers a variety of career opportunities, including the design and running of clinical trials and teaching.

Getting your clinical study designed and built ready for data collection takes A LOT of work and expertise… you’ve got to do all your CRF designs; keep up with protocol changes; add the ...

For Tammy Gusher Delgado, 56, the decision to join a clinical trial was clear. With a recent multiple sclerosis diagnosis and a clinical trial offering either the study drug or an approved ...

employing quality principles of current good clinical practice to produce valid and useful data Demonstrate sound ethical principles and values as they are recognized and upheld in research involving ...

Conference breakout session examines the role of strategic partnerships in driving progress for sexual and gender minority ...

Adaptive trial designs, utilising real-time data, present a solution to these challenges by refining trial design and ...