Clinical Trial Liaison (Ctl), Ophthalmology (Eu)
Pubblicato il 21-09-2026 - The Medical Affairs Company (Tmac) in Genova
pppTerritory will include multiple countries in the EU.
/p pServing as a value-added resource and extension of the Company the Clinical Trial Liaison (CTL) will support the company's Ophthalmology Neurology pipeline.
/p pThe CTL supports the execution of country medical plans related to clinical trial engagements.
/p pThe CTL will work tempo pieno to educate, analyze, and resolve issues with clinical research sites and investigators.
/p pThis 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.
/p h3Essential Duties And Responsibilities /h3 h3Site and Investigator Partnerships /h3 ul liCreate investigator engagement plans to support site identification and selection /li liBuild and maintain partnerships with potential PIs for company clinical trials /li liConduct compliant scientific exchange to educate on company clinical trials /li liProvide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers,
and clinical trial recruitment and retention /li liCollection of key medical insights from PIs to inform refinement of strategies /li liServe as a liaison to internal RD functions to ensure the effective support of PIs /li liRespond in a timely manner to unsolicited inquiries from external stakeholders and HCPs /li /ul h3Building Company Pipeline Advocacy /h3 ul liThrough compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships /li liCollect key strategic insights from top research KOLs and HCPs to support strategic initiatives /li liSupport execution of strategy through creation of national and regional congress plans for your assigned territories to attend and execute activities /li /ul h3Qualifications /h3 ul liAn advanced degree in life sciences (MD, PharmD or PhD or equivalent) required /li liHas established scientific relationships and the ability to deliver effective presentations to HCPs /li liExperience in clinical trial operations, design, site support and scientific engagement with clinical trial sites required.
/li liGeneral Ophthalmology or Anterior segment ophthalmology therapeutic area experience required /li liAt least 2 years of therapeutic, research or substantive patient care experience is required /li liFrequent travel is required.
Availability to travel up to 75% of time /li liAvailability to attend meetings on holidays and weekends /li liAbility to travel internationally as needed with valid passport /li liClean and valid driver's license /li /ul pClinical Trial Liaison (CTL), Ophthalmology (EU) genova, Italy /p /p #J-*****-Ljbffr