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Ph3Medical Science Liaison - Ophthalmology (Italy) /h3 pLocation: Savona, Liguria, Italy /p pPosted: /p pJob reference: f25501f7543b9b180e966e1a542be089 /p pThe Medical Affairs Company (TMAC) /p pbPosition Summary: /b 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. /p pbKey Responsibilities: /b /p ul liServe as a scientific expert, providing clinical and technical education to the ophthalmology community /li liSupport clinical trial awareness, enrollment, and retention for Client’s Phase III clinical trial study /li liDevelop and maintain collaborative relationships with thought leaders in academic, clinical, and healthcare organizations /li liContribute to corporate, scientific, and clinical strategies within the assigned region /li liParticipate in Medical Affairs initiatives to enhance overall company value and productivity /li /ul pbCore Duties: /b /p pb1. Scientific Expertise and Education /b /p ul liMaintain up-to-date knowledge in ophthalmology, specifically GA/Dry AMD /li liDeliver scientific presentations and support site initiation visits (SIVs) /li liRespond to unsolicited medical information requests /li /ul pb2. Clinical Trial Support /b /p ul liDrive awareness and enrollment for the Client’s Phase III clinical trial study /li liIdentify and recommend potential trial sites /li liAddress trial-related issues and overcome recruitment barriers /li /ul pb3. KOL Engagement /b /p ul liDevelop and execute KOL engagement plans /li liOrganize investigator meetings and recruitment events /li liProvide insights from KOL interactions to internal teams /li /ul pb4. Compliance and Reporting /b /p ul liAdhere to corporate SOPs and regulatory guidelines /li liDocument and report on field activities and KOL interactions /li /ul pb5. Cross-functional Collaboration /b /p ul liWork with Medical Affairs, Clinical Development, and Clinical Operations teams /li liSupport training of field and home office employees /li liParticipate in medical conferences and advisory board meetings /li /ul pbQualifications: /b /p ul liM.D., Ph.D., PharmD, DO, or equivalent terminal degree /li li2+ years of clinical experience in Ophthalmology /li liKnowledge of pharmaceutical industry regulations and compliance requirements /li li1+ years of MSL or Clinical Trial Liaison experience /li liExcellent communication and interpersonal skills /li liProficiency in English (additional languages may be required based on region) /li liValid driver's license and ability to travel up to 50% (including overnight stays) /li /ul pbPreferred Skills: /b /p ul liDemonstrated project management abilities /li liExperience working in cross-functional teams /li /ul pbPhysical Demands: /b 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. /p pbSalary: /b Offers to be determined based on industry experience, education, and therapeutic expertise. /p /p #J-18808-Ljbffr