ARTO are working with a Germany based Radiopharmaceutical company who are looking to expand their Global Medical Affairs team with an experienced Director. This person will be focused on the global publication strategy of their leading pipeline and marketed assets.SummaryLead the global medical publications strategy across an oncology and radiopharmaceutical portfolio, ensuring alignment with clinical development and evidence-generation priorities.Oversee the creation and execution of scientific publications including abstracts, manuscripts, posters, oral presentations, and omnichannel medical content.Shape and drive the global scientific narrative throughout the product lifecycle, supporting clinical adoption and healthcare decision‑making.Manage and develop a high‑performing Global Medical Affairs Publications team, setting strategic direction and performance expectations.Collaborate cross‑functionally with Medical Affairs, Clinical Development, Regulatory, Biostatistics, Dosimetry, and external stakeholders to ensure high‑quality scientific communication.Partner with investigators, key medical experts (KMEs), authors, journals, and publication agencies to deliver publications on time and in compliance with industry standards.Ensure all publication activities adhere to scientific integrity standards, publication ethics (ICMJE/GPP), FDA/ICH regulations, and transparency requirements.Oversee publication planning operations including timelines, budgets, vendor management, peer‑review coordination, and publication tracking systems.Qualifications & Candidate RequirementsAdvanced scientific degree required (MD, PharmD, or PhD) in oncology, nuclear medicine, or a related scientific discipline.3+ years’ experience leading Publications within Medical Affairs, ideally within oncology, radiopharmaceuticals, or specialty therapeutics.Strong background in publication management, medical writing, and clinical trial publications within biotech or pharma environments.Proven ability to work cross‑functionally in matrix organisations and engage effectively with investigators, authors, and key medical experts.Deep understanding of GCP, ICH guidelines, publication ethics, and medical compliance standards.Excellent scientific communication, project management, and stakeholder management skills with strong attention to detail.
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