As a Clinical Site Liaison, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
The Clinical Site Liaison is a field-based expert who supports the conduct and the patient recruitment of the client global clinical trials at investigative sites, through local and relational support.
What you will be doing: Participate in study-level feasibility activities through providing key country/regional and site-specific knowledge including patient pathways and operational execution.
Interface and act as a local client TrialOps representative, an expert on the clinical trial protocol(s) and SME providing the sites with knowledge and awareness about the current and upcoming clinical trials.
Lead and engage in local site, KOL and network engagement initiatives in view of the clinical trials.
Contribute to the trial-specific site feasibility/selection strategy and collaborate with the Clinical Trial Team (CTT) and CRO to support the site start-up process as needed.
Facilitate with the site contract negotiation/signature as needed.
Proactively work to fully understand all matters that impact the successful patient recruitment and high-quality conduct of the clinical trial at each site, e.g., the Principle Investigator (PI) and site preferences and best practices on clinical trials, standard of care treatments, competing studies, etc.
Ensure a supportive relationship with clinical sites and trial personnel.
Proactively work to fully understand the patient voice, preferences, and pathway(s).
Closely work with the client GPA team.
Speak to patient groups and support groups, live events and conferences as allowed by local/regional guidance.
May also attend live and virtual patient events to assist in responding to questions about client, the trial(s) and other information.
May participate in monitoring oversight activities such as accompanying the CRO CRA during site visits to ensure high-quality conduct and execution of the clinical trials according to the protocol and ICH GCP and local regulatory requirements.
Closely work together with the Medical Affairs colleagues, e.g., the MSLs to ensure optimal synergies in the respective site contacts and support.
Optimize site engagement for a specific trial to ensure site engagement and quality for the site-level enrollment and execution of every trial.
Oversee and track patient recruitment for the regional sites and proactively identify ways to prevent recruitment delays.
Proactively identify issues and look for solutions in the assigned clinical trial and timely escalate them to the respective study CTM, CODL, Global Head of Clinical Site Communication, Recruitment and Liaisons, Head of Trial Operations and/or Senior Management, as needed.
Identify efficiencies, best practices and lessons learnt and ensure they are shared across trials/indications/compounds.
Search for and embrace innovation.
El anuncio original lo puedes encontrar en Kit Empleo: https://www.kitempleo.es/empleo/128677049/clinical-site-liaison-c-782-madrid/?utm_source=html #J-18808-Ljbffr