Clinical Site Engagement Liaison is responsible for the management of clinical Investigators and sites being considered and/or participating in sponsor's clinical trials and / or Post Marketing Safety Studies; inclusive of Investigator / site identification and qualification, the timely delivery of clinical trial enrollment in accordance with scientific objectives, timely delivery of database locks, issues management at clinical trial sites, and ensuring inspection readiness at all times for assigned therapeutic area(s) within a region/country that enables global program delivery.

This is achieved by the Site Engagement Liaison's accountability for comprehensive Investigator and site management, leveraging of information/tools to make/have informed decisions and discussions, and high quality interactions with global clinical trial sites to drive to an unparalled customer experience. S/he is also responsible for oversight of vendor monitoring activities at clinical trial sites, including the identification, mitigation and escalation of significant findings and trends.

Clinical Investigator Management

• • Accountable for activities required at clinical trial sites and by investigators and site staff participating in sponsor's trials; inclusive of site identification and qualification, enrollment planning and execution, to database lock and close out
  • Accountable for comprehensive investigator management activities to ensure timely delivery of enrollment readiness, trial recruitment/enrollment and database locks; inclusive of performance management and issue mitigation, identification and resolution
  • Responsible for identifying potential opportunities to accelerate trial enrollment, while driving to an unparalleled clinical trial/customer experience
  • Accountable for the application of scientific, therapeutic area, and institutional/regional expertise to inform and ensure timely delivery of trial enrollment and quality data

Clinical Trial Management

• • Responsible for the development and implementation of applicable investigator / site risk plans to ensure delivery of clinical trial enrollment commitments and database locks
  • Ensure site and country level inspection readiness at all times
  • Leverage metrics to inform site/country/regional level decision making
  • Work with internal and external teams to remove barriers to trial execution at a site and/or country level

Business Management and Engagement

• • Establishes and develops strong professional relationships with active/potential clinical investigators to expand/maintain clinical research partnership opportunities and provide an unparalleled experience for participation in sponsor's clinical trials.
  • Cross functional collaboration and partnership to ensure alignment in priorities and deliver the portfolio
  • Perform targeted sites prospecting in alignment with portfolio strategy & priority
  • Maintain therapeutic and technical expertise to enable scientific discussions with the investigator and site personnel
  • Serve as an effective communication “bridge” between sites, third party vendors and the sponsor

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• Bachelor’s degree or equivalent in science or pharma
• Ability to travel to sites in Slovakia  for visits when required for meetings
• Minimum of 4 years experience in the pharmaceutical industry and/or clinical research and strong working knowledge of Good Clinical Practice
• CTM experience is welcomed as well as Senior CRA experience
• Therapeutic expertise and knowledge of the clinical research landscape; ability to acquire and maintain therapeutic expertise to support portfolio needs
• Strong self-management and organizational skills; ability to manage workload, set personal priorities and adjust as needed
• Demonstrated strategic agility & broad business acumen