Associate Director, Clinical Site Liaison

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients. The Associate Director, Clinical Site Liaison (CSL) is a field-based expert who supports the conduct and the patient recruitment of argenx global clinical trials at investigative sites, through local and relational support.The successful candidate will have clinical trial operational experience and deep understanding of patient pathways and trial recruitment. Proven expertise in engaging, building and maintaining excellent working relationships with country/region specific investigative sites, KOLs, site networks and Patient Advocacy groups (PAG). From within the Trial Operations (Trial Ops) team, closely work together with the clinical trial/ indication teams and with CROs and other vendors. Collaborate with the argenx Global Patient Advocacy (GPA) group, as well as, with the Medical Affairs group (MSLs).Roles and Responsibilities:Participate in neurology franchise and study-level feasibility activities through providing key country/ regional and site-specific knowledge including patient pathways and operational executionInterface and act as a local argenx TrialOps representative, an expert on the clinical trial protocol(s) and SME providing the sites with knowledge and awareness about the current and upcoming clinical trialsLead and engage in local site, KOL and network engagement initiatives in view of the clinical trialsContribute to the trial specific site feasibility / selection strategy and collaborate with the Clinical Trial Team (CTT) and CRO to support the site start-up process as neededFacilitate with the site contract negotiation/signature as needed, collaborate with the GloSaM groupProactively work to fully understand all matters that impact the successful patient recruitment and high-quality conduct of the clinical trial at each site, eg the Principal Investigator (PI) and site preferences and best practices on clinical trials, standard of care treatments, competing studies etc. Ensure a supportive relationship with clinical sites and trial personnelProactively work to fully understand the patient voice, preferences and pathway(s). Closely work with the argenx GPA team. Speak to patient groups and support groups, live events and conferences as allowed by local / regional guidance. May also attend live and virtual patient events to assist in responding to questions about argenx, the trial(s) and other information on Mode of Action (MOA)May participate in monitoring oversight activities such as accompanying the CRO CRA during site visits. This to ensure high quality conduct and execution of the clinical trials according to the protocol and ICH GCP and local regulatory requirementsClosely work together with the Medical Affairs colleagues, eg the MSLs to ensure optimal synergies in the respective site contacts and supportOptimize site engagement for a specific trial and across the neurology franchise to ensure site engagement and quality for the site-level enrollment and execution of every trialOversee and track patient recruitment for the regional sites and pro-actively identify ways to prevent recruitment delaysPro-actively identify issues and look for solutions in the assigned clinical trial and timely escalate them to the respective study CTM, CODL, Global Head of Clinical Site Communication, Recruitment and Liaisons, Head of Trial Operations and/or Senior Management, as neededIdentify efficiencies, best practices and lessons learnt and ensure they are shared across trials/indications/compoundsSearch for and embrace innovationMay be asked to provide input to the clinical development strategy/planParticipate in workstreams and provide input to procedures/SOPs/WIs and related documentsSkills and Competencies:Knowledge of ICH-GCP and other applicable legislationAbility to quickly understand complex neurological disease areas, treatments and clinical development plansUnderstand the healthcare therapeutic landscape, patient pathways and investigative sitesExcellent communication and presentation skills and relationship management of multiple stakeholders, internally and externally, including sites, KOLs, networks, PAGs, CROs and othersLeadership with the ability to overcome challenges, seek opportunities to remove barriers, influence without authorityHighly developed organizational skills, problem solving, analytic and able to prioritizeExperience with tools and systems for managing clinical studiesEducation, Experience and Qualifications:Bachelors degree, Scientific or health related field University degree - medical or para-medical (MD, Biology, Biomedical Sciences, Pharmacy, Veterinary etc.) or equivalent by experienceMinimum of 6 years of experience in Biotech / pharma preferably in roles including site engagement and / or clinical trial monitoring experienceValid drivers licenseAbility for travel nationally and occasional international travel.Experience in global clinical trials is a plusPrior experience in Neurology, Auto-immune and rare disease background#LI-RemoteAt argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@. Only inquiries related to an accommodation request will receive a response.PDN-9caa9d24-1436-48e6-a591-c856845aa1b3

Created: 2024-12-01