Clinical Trial Liaison (CTL), Ophthalmology (EU)
Pubblicato il 11-09-2026 - The Medical Affairs Company (Tmac) in Genova
pTerritory will include multiple countries in the EU. /ppbr/ppServing 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. /ppbr/ppThis 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. /ppbr/ppbEssential Duties And Responsibilities /b /ppbSite and Investigator Partnerships /b /pulliCreate investigator engagement plans to support site identification and selection /liliBuild and maintain partnerships with potential PIs for company clinical trials /liliConduct compliant scientific exchange to educate on company clinical trials /liliProvide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers,
and clinical trial recruitment and retention /liliCollection of key medical insights from PIs to inform refinement of strategies /liliServe as a liaison to internal RD functions to ensure the effective support of PIs /liliRespond in a timely manner to unsolicited inquiries from external stakeholders and HCPs /li /ulpbBuilding Company Pipeline Advocacy /b /pulliThrough compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships /liliCollect key strategic insights from top research KOLs and HCPs to support strategic initiatives /liliSupport execution of strategy through creation of national and regional congress plans for your assigned territories to attend and execute activities /li /ulpbQualifications /b /pulliAn advanced degree in life sciences (MD, PharmD or PhD or equivalent) required /liliHas established scientific relationships and the ability to deliver effective presentations to HCPs /liliExperience in clinical trial operations, design, site support and scientific engagement with clinical trial sites required. /liliGeneral Ophthalmology or Anterior segment ophthalmology therapeutic area experience required /liliAt least 2 years of therapeutic, research or substantive patient care experience is required /liliFrequent travel is required. Availability to travel up to 75% of time /liliAvailability to attend meetings on holidays and weekends /liliAbility to travel internationally as needed with valid passport /liliClean and valid driver’s license /li /ul