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Clinical Site Liaison
hace 1 mes
The Clinical Site Liaison (CSL) is a key member of our Trial Operations team, responsible for supporting the conduct and patient recruitment of global clinical trials at investigative sites. This role requires a strong understanding of clinical trial operations, patient pathways, and trial recruitment.
Key Responsibilities
Participate in neurology franchise and study-level feasibility activities, providing key country/region and site-specific knowledge, including patient pathways and operational execution.
Interface with investigative sites, providing them with knowledge and awareness about current and upcoming clinical trials, and serving as a local TrialOps representative.
Lead and engage in local site, KOL, and network engagement initiatives to support clinical trials.
Contribute to trial-specific site feasibility/selection strategy and collaborate with the Clinical Trial Team (CTT) and CRO to support site start-up processes.
Facilitate site contract negotiation and signature, collaborate with the GloSaM group, and proactively work to understand matters impacting successful patient recruitment and high-quality conduct of clinical trials at each site.
Closely work with the Global Patient Advocacy (GPA) team and may participate in monitoring oversight activities, such as accompanying the CRO CRA during site visits.
Optimize site engagement for specific trials and across the neurology franchise, oversee and track patient recruitment for regional sites, and proactively identify ways to prevent recruitment delays.
Identify issues and look for solutions in assigned clinical trials, timely escalating them as needed, and ensure that efficiencies, best practices, and lessons learned are shared across trials/indications/compounds.
Search for and embrace innovation, and may be asked to provide input to the clinical development strategy/plan.
Participate in workstreams and provide input to procedures/SOPs/WIs and related documents.
Requirements
Bachelor's degree in a scientific or health-related field.
Minimum of 6 years of experience in Biotech/pharma, preferably in roles including site engagement and/or clinical trial monitoring experience.
Valid driver's license and ability for travel nationally and occasional international travel.
Experience in global clinical trials is a plus, and prior experience in Neurology, Auto-immune, and rare disease background is highly valued.
What We Offer
Thermo Fisher Scientific offers a dynamic and challenging work environment, with opportunities for professional growth and development. We are committed to providing our employees with the resources and support they need to succeed in their roles and advance in their careers.
