
51 - 200 employés
🧬 Biotechnologie
💊 Pharmaceutique
💰 €149 000 000 Series B en 2022-12
Biotechnology • Pharmaceuticals
Apogee Therapeutics est une entreprise de biotechnologie en phase clinique spécialisée dans le développement de nouveaux produits biologiques pour le traitement des troubles inflammatoires et immunologiques. La société cible les principaux marchés des maladies inflammatoires et immunitaires telles que la dermatite atopique, l'asthme, la bronchopneumopathie chronique obstructive, l'œsophagite à éosinophiles et d'autres conditions connexes. Apogee Therapeutics cherche à redéfinir les normes de soins actuelles en faisant progresser les traitements par anticorps visant des mécanismes biologiques bien établis, avec le potentiel de traiter les problèmes dermatologiques, respiratoires et gastro-entérologiques. L'entreprise s'engage à créer un environnement de travail psychologiquement sûr tout en priorisant des options de traitement innovantes pour ceux qui vivent avec ces affections.
🕒 il y a 2 mois
🗣️🇺🇸🇬🇧 Anglais requis
Améliorez vos chances d'obtenir un entretien en vérifiant votre score de CV avant de postuler.

51 - 200 employés
🧬 Biotechnologie
💊 Pharmaceutique
💰 €149 000 000 Series B en 2022-12
Biotechnology • Pharmaceuticals
Apogee Therapeutics est une entreprise de biotechnologie en phase clinique spécialisée dans le développement de nouveaux produits biologiques pour le traitement des troubles inflammatoires et immunologiques. La société cible les principaux marchés des maladies inflammatoires et immunitaires telles que la dermatite atopique, l'asthme, la bronchopneumopathie chronique obstructive, l'œsophagite à éosinophiles et d'autres conditions connexes. Apogee Therapeutics cherche à redéfinir les normes de soins actuelles en faisant progresser les traitements par anticorps visant des mécanismes biologiques bien établis, avec le potentiel de traiter les problèmes dermatologiques, respiratoires et gastro-entérologiques. L'entreprise s'engage à créer un environnement de travail psychologiquement sûr tout en priorisant des options de traitement innovantes pour ceux qui vivent avec ces affections.
• Lead and coordinate interactions with project teams, clinical study teams, management, consultants, and collaborators to facilitate timely acceptance/approval of regulatory submissions including INDs, CTAs, NDAs, BLAs, and PIPs/PSPs, among others • Support the data collection and cross-functional authorship for regulatory documents. Proofread, edit, and prepare documents for inclusion in regulatory submissions; coordinate with multiple departments to obtain content needed for submissions • Communicate timelines for regulatory submissions to individuals and departments and follow up to ensure timely submission • Serve as the primary interface with regulatory publishing to ensure compliant electronic submissions to FDA, and ex-US regulatory agencies as needed • Appropriately archive and maintain regulatory submissions and correspondences in Apogee’s regulatory information management system • Implement and maintain use of standardized templates and guidelines for documentation to be included in regulatory submissions; provide formatting assistance and advice to team members • With mentoring and guidance from the regulatory affairs leadership team, understand and communicate US and international regulatory requirements to ensure quality documents are submitted either directly or in collaboration with a CRO or corporate partner • Support global regulatory leads on clinical study and execution teams to ensure that clinical trial deliverables, timelines, and objectives are met
• BS/MS/PhD (or equivalent) in regulatory affairs or related scientific discipline • Regulatory Affairs Certification (RAC) credential preferred • A minimum of 5 years of regulatory experience working in drug development in the biopharmaceutical industry • Experience interacting with health authorities including FDA and EMA • Strong project management skills with a high sense of urgency, ability to collaborate and influence effectively cross-functionally • Strong communication skills with an ability to present to a variety of stakeholders and tailor message accordingly • Experience working in Veeva Regulatory Information Management (RIM) platforms, eCTD submissions, and Microsoft Office SharePoint/Teams • Successfully exhibit Apogee’s C.O.R.E. values: Caring, Original, Resilient and Egoless • Position requires up to 10% travel including mandatory in-person attendance at All Hands meetings typically held twice per year
• A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless • Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly • Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits • We provide competitive time off, including three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave • Commitment to growing you professionally and providing access to resources to further your development • Apogee offers regular all team, in-person meetings to build relationships and problem solve
Postuler Maintenant🕒 il y a 2 mois
Senior Associate, Compliance as a Service at Aprio. Join a top 20 CPA firm focusing on compliance for clients.
🇺🇸 États-Unis – Télétravail
💵 $80 000 - $132 000 / an
💰 Debt Financing en 2018-10
⏰ Temps Plein
🟠 Senior
🚔 Conformité
🦅 Parrain de Visa H1B
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 2 mois
Compliance Analyst at Thimble, ensuring regulatory compliance for insurance products. Collaborating with teams to uphold compliance standards and improve operational efficacy.
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 2 mois
Compliance Engineer responsible for implementing and maintaining technical security controls for CyberSheath. Collaborating with teams and supporting CMMC compliance for clients.
🇺🇸 États-Unis – Télétravail
💵 $100 000 - $116 000 / an
💰 Private Equity Round en 2021-12
⏰ Temps Plein
🟡 Intermédiaire
🟠 Senior
🚔 Conformité
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 2 mois
Manager overseeing compliance and reporting analytics for a healthcare organization. Leading a team while ensuring regulatory alignment and performance monitoring across operations and delegates.
🇺🇸 États-Unis – Télétravail
💵 $130 332 - $195 498 / an
💰 €321 050 000 Post-IPO Debt - Alignment Health en 2024-11
⏰ Temps Plein
🟡 Intermédiaire
🟠 Senior
🚔 Conformité
🗣️🇺🇸🇬🇧 Anglais requis
🕒 il y a 2 mois
Business Line Compliance Officer at Performance Trust providing compliance advisory support for Investment Banking and Capital Markets. Seeking candidates with regulatory guidance experience and strong analytical skills.
🗣️🇺🇸🇬🇧 Anglais requis