20 set - Torino
The Medical Affairs Company (Tmac)
p Territory will include multiple countries in the EU. p Scopra di più sui compiti quotidiani, le responsabilità generali e l'esperienza richiesta per questa occasione scorrendo subito verso il basso. brp 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 full time to educate, analyze, and resolve issues with clinical research sites and investigators. /p p 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. /p pb Essential Duties And Responsibilities /b /ppb Site and Investigator Partnerships /b /pulli Create investigator engagement plans to support site identification and selection /lili Build and maintain partnerships with potential PIs for company clinical trials /lili Conduct compliant scientific exchange to educate on company clinical trials /lili Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers,
and clinical trial recruitment and retention /lili Collection of key medical insights from PIs to inform refinement of strategies /lili Serve as a liaison to internal RD functions to ensure the effective support of PIs /lili Respond in a timely manner to unsolicited inquiries from external stakeholders and HCPs /li /ulpb Building Company Pipeline Advocacy /b /pulli Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships /lili Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives /lili Support execution of strategy through creation of national and regional congress plans for your assigned territories to attend and execute activities /li /ulpb Qualifications /b /pulli An advanced degree in life sciences (MD, PharmD or PhD or equivalent) required /lili Has established scientific relationships and the ability to deliver effective presentations to HCPs /lili Experience in clinical trial operations, design, site support and scientific engagement with clinical trial sites required. xrdbqlu /lili General Ophthalmology or Anterior segment ophthalmology therapeutic area experience required /lili At least 2 years of therapeutic, research or substantive patient care experience is required /lili Frequent travel is required. Availability to travel up to 75% of time /lili Availability to attend meetings on holidays and weekends /lili Ability to travel internationally as needed with valid passport /lili Clean and valid driver’s license /li /ul /p /p
21 set - Arezzo
Adecco
21 set - Milano
Salute
21 set - Milano
OPENJOBMETIS
21 set - Bologna
Unipol Group