Associate Director - Clinical Site Liaison

6 days ago

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argenx

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Oncology • Autoimmune diseases • Rare Diseases • Antibody based medicines • Immunotherapy

1001 - 5000

Description

• Participate in neurology franchise and study-level feasibility activities through providing key country/ regional and site-specific knowledge including patient pathways and operational execution • Interface 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 trials • Lead and engage in local site, KOL and network engagement initiatives in view of the clinical trials • Contribute 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 needed • Facilitate with the site contract negotiation/signature as needed, collaborate with the GloSaM group • Proactively 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 personnel • Proactively 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. • Participate in monitoring oversight activities such as accompanying the CRO CRA during site visits.

Requirements

• Bachelor’s degree, Scientific or health related field • University degree – medical or para-medical (MD, Biology, Biomedical Sciences, Pharmacy, Veterinary etc.) or equivalent by experience • Minimum of 6 years of experience in Biotech / pharma preferably in roles including site engagement and / or clinical trial monitoring experience • Valid driver’s license • Ability for travel nationally and occasional international travel. • Experience in global clinical trials is a plus • Prior experience in Neurology, Auto-immune and rare disease background