17 set - Udine
The Medical Affairs Company (Tmac)
ph3Descrizione dell’offerta di lavoro /h3 pTerritory 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. 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. /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 /p #J-18808-Ljbffr
18 set - Chiavari
Acrobatica
18 set - Fonzaso
Greta
18 set - Trento
Car Clinic
18 set - Nola
Demetra Formazione