Patient and Site engagement liaison

pExcelya Amsterdam, North Holland, Netherlands /ph3Patient and Site Engagement Liaison /h3pstrongExcelya /strong /ppCreated in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. /ppWe offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our +800 Excelyates. /ppOur unique one-stop provider service model – leveraging full-service, functional service provider and consulting – allows our Excelyates to evolve through a diverse array of projects. /ppIn collaboration with preeminent experts, Excelya advances scientific, managerial and human knowledge to improve the patient journey. /ppFor our team members, excelling with care means benefitting from a stimulating professional environment that encourages personal, intellectual, and operational participation so that together we can be the best in our field. /ppWe commit to giving each Excelyate the means to express their natural talents, develop their full potential and invest their unique selves in our unique project. /ppstrongThe role: /strong /pulliYou are accountable to build and maintain clinical site relationships (i.e. with investigators, site staff, External Experts, Patient Organizations etc.) and internal stakeholders for global clinical development programs across different therapeutic areas. /liliYou identify opportunities that create competitive advantage and drive clinical development excellence in the country to increase value, efficiency and speed. /liliYou develop the clinical trial site and patient engagement strategy in the country, in full alignment with the regional Project Manager. /liliYou provide guidance in how to set-up patient site engagement initiatives based on established local working guidelines. /li /ulpstrongWhat you should bring to the team: /strong /pulliStrong clinical trial management experience with emphasis on teamwork to ensure collaboration in stakeholders management. /liliUnderstanding of local/regional major regulations including the local rules and regulations of engaging with patients and HCPs (compliance framework). /liliPrevious experience in working with CROs and POs is nice to have. /liliAbility to build and maintain strong relationships of mutual value. /liliExcellent influencing and communication skills. /li /ulpPlease note you will strongneed to be based in the Netherlands /strong when working in this role (fully remote working is not possible). This is a hybrid position. /ppPlease contact me for further details on /ph3Seniority level /h3pAssociate /ph3Employment type /h3pFull-time /ph3Job function /h3pConsulting, Research, and Strategy/Planning /ph3Industries /h3pPharmaceutical Manufacturing /p #J-18808-Ljbffr