.This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description The Clinical Site Liaison (CSL) is a field based expert who supports the conduct and the patient recruitment of global clinical trials at investigative sites, through local and relational support.The successful candidate will have clinical trial operational experience and deep understanding of patient pathways and trial recruitment.Proven expertise in engaging, building and maintaining excellent working relationships with country / region specific investigative sites, KOLs, site networks and Patient Advocacy groups (PAG).From within the Trial Operations (Trial Ops) team, closely work together with the clinical trial/ indication teams and with CROs and other vendors.Collaborate with the Global Patient Advocacy (GPA) group as well as with the Medical Affairs group (MSLs).ROLES AND RESPONSIBILITIES The CSL responsibilities include: Participate in neurology franchise and 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 Trial Ops 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, collaborate with the Glo Sa M group Proactively work to fully understand all matters that impact the successful patient recruitment and high quality conduct of the clinical trial at each site, eg the Principal 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 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 the client, the trial(s) and other information on Mode of Action (MOA).May participate in monitoring oversight activities such as accompanying the CRO CRA during site visits.This to ensure high quality conduct and execution of the clinical trials according to the protocol and ICH GCP and local regulatory requirements
