Medical Science Liaison, Ophthalmology (Italy)
Jobtome
Medical Science Liaison - Ophthalmology (Italy)Location: Savona, Liguria, ItalyPosted: 19.05.2026Job reference: f25501f7543b9b180e966e1a542be089The Medical Affairs Company (TMAC)Position Summary: As a field-based extension of our Client’s Medical Affairs team, the Medical Science Liaison (MSL) will support our Client’s investigational compound currently in Phase III clinical trial for dry AMD/Geographic Atrophy (GA). The MSL will establish and maintain scientific relationships with key opinion leaders (KOLs), investigators, and healthcare professionals in the ophthalmology field, particularly those specializing in retinal diseases.Key Responsibilities:
Serve as a scientific expert, providing clinical and technical education to the ophthalmology communitySupport clinical trial awareness, enrollment, and retention for Client’s Phase III clinical trial studyDevelop and maintain collaborative relationships with thought leaders in academic, clinical, and healthcare organizationsContribute to corporate, scientific, and clinical strategies within the assigned regionParticipate in Medical Affairs initiatives to enhance overall company value and productivity
Core Duties:1. Scientific Expertise and Education
Maintain up-to-date knowledge in ophthalmology, specifically GA/Dry AMDDeliver scientific presentations and support site initiation visits (SIVs)Respond to unsolicited medical information requests
2. Clinical Trial Support
Drive awareness and enrollment for the Client’s Phase III clinical trial studyIdentify and recommend potential trial sitesAddress trial-related issues and overcome recruitment barriers
3. KOL Engagement
Develop and execute KOL engagement plansOrganize investigator meetings and recruitment eventsProvide insights from KOL interactions to internal teams
4. Compliance and Reporting
Adhere to corporate SOPs and regulatory guidelinesDocument and report on field activities and KOL interactions
5. Cross-functional Collaboration
Work with Medical Affairs, Clinical Development, and Clinical Operations teamsSupport training of field and home office employeesParticipate in medical conferences and advisory board meetings
Qualifications:
M.D., Ph.D., PharmD, DO, or equivalent terminal degree2+ years of clinical experience in OphthalmologyKnowledge of pharmaceutical industry regulations and compliance requirements1+ years of MSL or Clinical Trial Liaison experienceExcellent communication and interpersonal skillsProficiency in English (additional languages may be required based on region)Valid driver's license and ability to travel up to 50% (including overnight stays)
Preferred Skills:
Demonstrated project management abilitiesExperience working in cross-functional teams
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Salary: Offers to be determined based on industry experience, education, and therapeutic expertise.#J-18808-Ljbffr
Serve as a scientific expert, providing clinical and technical education to the ophthalmology communitySupport clinical trial awareness, enrollment, and retention for Client’s Phase III clinical trial studyDevelop and maintain collaborative relationships with thought leaders in academic, clinical, and healthcare organizationsContribute to corporate, scientific, and clinical strategies within the assigned regionParticipate in Medical Affairs initiatives to enhance overall company value and productivity
Core Duties:1. Scientific Expertise and Education
Maintain up-to-date knowledge in ophthalmology, specifically GA/Dry AMDDeliver scientific presentations and support site initiation visits (SIVs)Respond to unsolicited medical information requests
2. Clinical Trial Support
Drive awareness and enrollment for the Client’s Phase III clinical trial studyIdentify and recommend potential trial sitesAddress trial-related issues and overcome recruitment barriers
3. KOL Engagement
Develop and execute KOL engagement plansOrganize investigator meetings and recruitment eventsProvide insights from KOL interactions to internal teams
4. Compliance and Reporting
Adhere to corporate SOPs and regulatory guidelinesDocument and report on field activities and KOL interactions
5. Cross-functional Collaboration
Work with Medical Affairs, Clinical Development, and Clinical Operations teamsSupport training of field and home office employeesParticipate in medical conferences and advisory board meetings
Qualifications:
M.D., Ph.D., PharmD, DO, or equivalent terminal degree2+ years of clinical experience in OphthalmologyKnowledge of pharmaceutical industry regulations and compliance requirements1+ years of MSL or Clinical Trial Liaison experienceExcellent communication and interpersonal skillsProficiency in English (additional languages may be required based on region)Valid driver's license and ability to travel up to 50% (including overnight stays)
Preferred Skills:
Demonstrated project management abilitiesExperience working in cross-functional teams
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential function of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Salary: Offers to be determined based on industry experience, education, and therapeutic expertise.#J-18808-Ljbffr
Offerta di lavoro pubblicata 10 ore fa
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