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Clinical Site Liaison

1 mese fa

Milano, Lombardia, Italia Pharmiweb A tempo pieno
Clinical Site Liaison Job Description

As a Clinical Site Liaison at Pharmiweb, you will be part of the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence. Your role will be to support the conduct and patient recruitment of global clinical trials at investigative sites through local and relational support.

Key Responsibilities:
  • Study-Level Feasibility: Provide key country, regional, and site-specific knowledge, including patient pathways and operational execution.
  • Local Client TrialOps Representative: Interface with sites, providing knowledge and awareness about current and upcoming clinical trials.
  • Site Engagement: Lead and engage in local site, KOL, and network engagement initiatives for clinical trials.
  • Site Feasibility/Selection Strategy: Contribute to trial-specific site feasibility and selection strategy, collaborating with the Clinical Trial Team and CRO.
  • Site Contract Negotiation: Facilitate site contract negotiation and signature as needed.
  • Patient Recruitment and Site Quality: Proactively work to understand matters impacting successful patient recruitment and high-quality conduct of clinical trials at each site.
  • Patient Voice and Pathways: Understand patient voice, preferences, and pathways, working closely with the client GPA team.
  • Monitoring Oversight: Participate in monitoring oversight activities, ensuring high-quality conduct and execution of clinical trials.
  • Site Engagement and Quality: Optimize site engagement for specific trials, ensuring site-level enrollment and execution.
  • Patient Recruitment Tracking: Oversee and track patient recruitment for regional sites, identifying ways to prevent recruitment delays.
  • Issue Identification and Escalation: Proactively identify issues and escalate them to the respective study CTM, CODL, and senior management as needed.
  • Efficiency, Best Practices, and Lessons Learned: Identify efficiencies, best practices, and lessons learned, ensuring they are shared across trials, indications, and compounds.
Requirements:
  • Education: Bachelor's degree in a scientific or health-related field, or equivalent by experience.
  • Experience: Minimum of 6 years of experience in biotech/pharma, preferably in roles including site engagement and/or clinical trial monitoring.
  • Travel: Ability to travel nationally and occasionally internationally.
  • Global Clinical Trials Experience: Experience in global clinical trials is a plus.
  • Neurology, Autoimmune, and Rare Disease Background: Prior experience in neurology, autoimmune, and rare disease background is a plus.
  • ICH-GCP and Legislation: Knowledge of ICH-GCP and other applicable legislation.
  • Communication and Presentation Skills: Excellent communication and presentation skills, with the ability to manage multiple stakeholders.
  • Leadership and Problem-Solving: Leadership skills, with the ability to overcome challenges and prioritize tasks.
What ICON Can Offer:

Our success depends on the quality of our people. We offer a range of benefits, including competitive salary, annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.