Pleased to meet you, we are Galapagos, a dynamic growing Biotech company with offices across Europe and in US, headquartered in Mechelen, Belgium.

We are in the business of changing lives. Focusing on high unmet medical needs, we synergize compelling science, technology, and collaborative approaches to create a deep pipeline of best-in-class medicines. With capabilities from lab to patient, including a decentralized cell therapy manufacturing platform, we are committed to challenging the status quo and delivering results for our patients, employees, and shareholders. Our goal is not just to meet current medical needs but to anticipate and shape the future of healthcare, ensuring that our innovations reach those who need them most.

We pioneer for patients. We need thought leaders and rapid thinkers, entrepreneurs in spirit and status quo-fighters. Collaborative innovators and perseverant idealists. We need the best-in-class. In other words, we need you : The ‘make-it-happener’.

We are looking for an Associate Medical Director - Cell Therapy

Scope of the job

This is a hybrid position that will provide medical strategic input and will perform functional (operational) activities in support of core medical affairs initiatives in the US and in assigned region. This role is responsible for the US Medical Affairs strategic and tactical planning in coordination with other cross-functional teams and tactical execution of core medical affairs activities including: Evidence generation, HCP and stakeholder interactions (clinical trials, prescribers/providers, KOL development, patient groups, payers), insight capture (advisory boards, steering committees, CI), interpretation of clinical and scientific data, real-world data analyses, and educational initiatives (medical education, value proposition/dossier).

Your role

• Build and maintain strong relationships with key US Investigators, Thought Leaders (TLs), healthcare professionals, and patient advocacy groups to gather insights, drive advocacy and ensure our therapies meet the needs of patients and healthcare providers
• Execute on the US Medical Affairs strategy and programs in the assigned area to include meeting with key stakeholders and partners (both in person and via Teams/Zoom).
• Participate in the development of the US Medical Affairs strategy in support of the company's goals through collaboration with Clinical Development, Commercial Strategy, Regulatory, HEOR, and other cross functional teams both in the US and BE.
• Support enrollment, and execution, of key Galapagos clinical trials across pipeline assets
• Identify and lead and execute disease regional strategies and tactics by securing insights via external engagements with Academic and Hospital physicians, 1:1 HCPs and investigators at local scientific meetings and national and international medical congresses
• Represent US Medical Affairs as cell therapy or therapeutic area expert in Oncology/Heme-Onc both internally and externally
• Provide input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, advisory board meeting materials, and medical information response documents, etc.
• Ensure the effective dissemination of the data generated through generation of publication plan, congress strategy plan, Medical Information response, CME/IME plans in conjunction with respective cross-functional partners
• Use expertise in cell therapy, clinical trials, and disease state knowledge to provide input in advancing pipeline assets, clinical trial designs, and providing strategic medical input to cross-functional partners
• Continually monitor and perform an assessment/analysis on scientific communications platforms, scientific narratives, and related communications, with regard to the US medical strategic plan, and report data gaps
• Stay updated on latest developments and competitive landscape in the therapeutic area, US healthcare market, and particularly within oncology and cell therapy.
• Internally represent US Medical Affairs at steering committees, cross-functional teams, clinical development teams
• Create and support medical Information response documents, scientific educational grant requests and patient advocacy grant requests etc.
• Serve as reviewer on external communication materials as part of Medial, Legal, Regulatory (MLR) review team