Identification: 5016
Credits: None available.
Identification: 5058
Credits: None available.
Identification: 128
Credits: None available.
Identification: 131
Credits: None available.
Identification: 125
Credits: None available.
Identification: 176
Credits: None available.
Virginia Nido and Julia Medina will co-present on our personal experience cultivating asponsor/protégé relationship over many years. Virginia is an executive director at Genentech and Julia is an administrative assistant, aspiring to be a clinical research associate. We will discuss how and why we started and are committed to continuing a sponsor/protégé relationship, the advantages and challenges we have faced, and our responsibilities to each other.
Identification: 5028
Credits: None available.
Identification: 106
Credits: None available.
This session will address the challenge around how to implement a centralized feasibility process and assess a study protocol and know whether or not your institution should participate in the study. This is important for the audience to learn because assessing a feasibility process is essential and the last thing someone wants to do is agree to participate in a study that does not align with their institution's values or would not be a successful study for their site to participate in. The audience will walk away with tools needed to implement a centralized feasibility process.
Identification: 116
Credits: None available.
Identification: 139
Credits: None available.
The core quality area of discussion will include Quality Oversight of clinical trial conduct, data, and patient safety during remote monitoring. Audience will be provided with tips to prioritize remote monitoring activities, to engage site staff and PI during remote monitoring and example of remote monitoring tools.