Global Regulatory Strategy Lead, Late-Stage Biotech Phase 3
Avalo Therapeutics, Inc.
Avalo Therapeutics, Inc. in Pennsylvania is seeking a strategic Director of Regulatory Affairs to provide global regulatory leadership for the product abdakibart (AVTX-009) as it progresses into Phase 3 and beyond. The role includes designing regulatory strategies, leading submission processes, and collaborating with senior regulatory leadership. The ideal candidate should have 10–15 years of experience in Regulatory Affairs within the biotechnology or pharmaceutical sector, with at least 5 years at a small or emerging company. A bachelor’s degree in a scientific discipline is required, and advanced degrees are preferred. #J-18808-Ljbffr Avalo Therapeutics, Inc.
$380k - $420k
...President, Asset Strategy Lead, Revumenib At Syndax... ...is a commercial stage biopharmaceutical... ...Lead (ASL), Late Development provides... ...operational excellence in global oncology product... ...programs through regulatory approval and... ...asset with an ongoing Phase 3 program, ensuring...RegulatoryFull timeWork at officeLocal area- ...Senior Director, Biostatistics to lead statistical strategy and deliverables for late-stage programs. This role combines... ...in study design, analyses, and regulatory interactions, with oversight of... ...outsourced model, collaborating with global teams and #J-18808-Ljbffr...Regulatory
$256.07k - $336.1k
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...prior experience of leading the launch of CPG... ...CPG innovation stage-gate processes, identifying... ...-gate nuances, regulatory checkpoints, and... ...CPG innovation strategies. Provide leadership... ...launched within global CPG companies. Strong... ...40.00-$200,000.00 3 days ago New...RegulatoryHourly payFull timeLocal area- ...President, Marketing & Global Brand to own... ...s global brand strategy and marketing... ...Affairs, and Regulatory to ensure the... ...international markets Lead brand... ...pre-commercial biotech environment ~... ...Immunic is a late-stage biotechnology company... ...currently in phase 3 clinical...RegulatoryFull timeLocal areaFlexible hours
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