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Clinical Site Liaison Specialist
2 months ago
We are seeking a highly skilled Clinical Site Liaison to join our team at Lifelancer, a talent-hiring platform in Life Sciences, Pharma, and IT. As a Clinical Site Liaison, you will play a critical role in supporting the conduct and patient recruitment of global clinical trials at investigative sites.
Key Responsibilities:- Participate in feasibility activities, providing key country/region-specific knowledge, patient pathways, and operational execution.
- Interface with sites, KOLs, networks, and Patient Advocacy groups, providing expertise on clinical trial protocols and SME knowledge.
- Lead 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 and CRO to support site start-up.
- Facilitate site contract negotiation and collaboration with the GloSaM group.
- Proactively understand site preferences, best practices, and competing studies to ensure successful patient recruitment and high-quality conduct.
- Work closely with the Global Patient Advocacy team, speaking to patient groups, and attending live and virtual events to respond to questions about the client, trial(s), and Mode of Action.
- Participate in monitoring oversight activities, ensuring high-quality conduct and execution of clinical trials according to protocol and ICH GCP and local regulatory requirements.
- Closely work with Medical Affairs colleagues to ensure optimal synergies in site contacts and support.
- Optimize site engagement for specific trials and across the neurology franchise to ensure site-level enrollment and execution.
- Oversee and track patient recruitment for regional sites, proactively identifying ways to prevent recruitment delays.
- Identify issues, look for solutions, 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.
- Identify efficiencies, best practices, and lessons learned, ensuring they are shared across trials/indications/compounds.
- Search for and embrace innovation.
- Provide input to the clinical development strategy/plan and participate in workstreams, providing input to procedures/SOPs/WIs and related documents.
- Bachelor's degree in a scientific or health-related field, or equivalent by experience.
- Minimum 6 years of experience in Biotech/Pharma, preferably in roles including site engagement and/or clinical trial monitoring.
- Valid driver's license and ability for national and occasional international travel.
- Experience in global clinical trials and prior experience in Neurology, Auto-immune, and rare disease background are a plus.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma, and IT. We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains. Please use the below Lifelancer link for job application and quicker response.
