Clinical Trial Liaisons

Clinical Trial Liaisons (CTLs) are highly trained, experienced professionals, who provide communications to thought leaders, study sites and referral centers during clinical drug development. CTLs can be a driving force to ensure sites are enrolling patients in key clinical trials.

CTLs Role Responsibilities:

Clinical Trial Liaison (CTL) value explained from three stakeholder perspectives:

Clinical Trial Site Support

CTLs can conduct “Site Investigator Meetings” with each clinical trial site to ensure there is comprehension of the intricacies of the study and sustained enthusiasm throughout the enrollment period of the trial. Clinical Trial Liaisons can present the protocol, interim data, enrollment updates, and other information that is pertinent to the sites.

They can troubleshoot issues along with the contract research organization (CRO) and bring rapid feedback from the sites to the home office.

Insights generated by CTLs can help shape the clinical development program.

CTLs visiting clinical trial sites will typically visit them at least quarterly, and in some cases every 4-8 weeks. Site visit frequency is determined by the progress of enrollment and level of support needed by the sites.

Clinical Trial Referral Support

MSLs can ensure referral sites are aware of the clinical trial and refer potential patients to key clinical trials.

 

Case Studies

Case Study: Contract CTLs Supporting Clinical Trials

A large biotechnology company wanted to deploy a team of 30 CTLs and three managers in support of the launch of a novel oncology supportive care product.

The team was deployed in 6 weeks and trained and certified field ready in 3 weeks.

The team conducted quarterly Site Investigator Meetings to provide education, guidance and inspiration to the trial sites.

Those sites that were visited by a Clinical Trial Liaison enrolled 30-40% more patients than those that were not. The CTLs demonstrated a return on education after only a few months.