Clinical Trial Liaison
Pubblicato il 09-09-2026 - The Medical Affairs Company (Tmac) in Frosinone
Territory will include multiple countries in the EU.Ha le carte in regola per avere successo? Le seguenti informazioni devono essere lette attentamente da tutti i candidati.Serving as a value-added resource and extension of the Company the Clinical Trial Liaison (CTL) will support the company's Ophthalmology & Neurology pipeline. The CTL supports the execution of country medical plans related to clinical trial engagements. The CTL will work tempo pieno to educate, analyze, and resolve issues with clinical research sites and investigators.This role involves compliant collaboration with KOLs, investigators, research staff members, advocacy groups to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension to support the company's clinical trial programs.Essential Duties And ResponsibilitiesSite and Investigator PartnershipsCreate investigator engagement plans to support site identification and selectionBuild and maintain partnerships with potential PIs for company clinical trialsConduct compliant scientific exchange to educate on company clinical trialsProvide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers,
and clinical trial recruitment and retentionCollection of key medical insights from PIs to inform refinement of strategiesServe as a liaison to internal R&D; functions to ensure the effective support of PIsRespond in a timely manner to unsolicited inquiries from external stakeholders and HCPsBuilding Company & Pipeline AdvocacyThrough compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnershipsCollect key strategic insights from top research KOLs and HCPs to support strategic initiativesSupport execution of strategy through creation of national and regional congress plans for your assigned territories to attend and execute activitiesQualificationsAn advanced degree in life sciences (MD, PharmD or PhD or equivalent) requiredHas established scientific relationships and the ability to deliver effective presentations to HCPsExperience in clinical trial operations, design, site support and scientific engagement with clinical trial sites required. xrtlpzc General Ophthalmology or Anterior segment ophthalmology therapeutic area experience requiredAt least 2 years of therapeutic, research or substantive patient care experience is requiredFrequent travel is required. Availability to travel up to 75% of timeAvailability to attend meetings on holidays and weekendsAbility to travel internationally as needed with valid passportClean and valid driver’s license