Patient Operations Management Associate – Contract

🕒 il y a 2 mois

🏄 California – Distant

🏄 California – Remote

💵 $50 - $60 / heure

⏳ Contrat

🟢 Junior

🟡 Intermédiaire

⚙️ Opérations

👻 Score fantôme 21%

Ce que ça veut dire : la probabilité que personne ne recrute vraiment pour cette offre.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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Allogene Therapeutics

Site WebLinkedInTous les Emplois

201 - 500 employés

Fondée en 2017

🧬 Biotechnologie

💊 Pharmaceutique

Biotechnology • Pharmaceuticals

Allogene Therapeutics est une entreprise de biotechnologie en phase clinique, dont le siège est situé à South San Francisco. Elle développe des thérapies à base de cellules T à récepteur antigénique chimérique allogénique (AlloCAR T) pour le traitement du cancer et des maladies auto-immunes. L'entreprise se concentre sur l'immunothérapie et l'oncologie, exploitant des approches de CAR T prêtes à l'emploi pour créer des produits de thérapie cellulaire allogénique ciblant les maladies hématologiques malignes et potentiellement les indications auto-immunes.

Description

• Manage patient scheduling tools, guidelines, work instructions, and dashboards for cell therapy product delivery • Support tracking and reporting investigational product logistics information and patient metrics using databases, spreadsheets, and other tools • Support communication plans and templates for regular updates with Clinical Operations and clinical sites on patient status • Handle manuals and training materials for clinical sites regarding patient material shipping and product receipt • Support investigational product logistics and supply chain processes for domestic and international clinical trial activities • Support management of vendors and systems associated with investigational product logistics with cross-functional stakeholders • Participate in meetings supporting clinical trial launches and ongoing enrollment activities • Collaborate with key stakeholders to ensure a thorough patient journey program • Recommend process improvements and promote collaboration and execution excellence • Provide training to CRO staff, clinical site staff, and other audiences as needed • Participate in the development, review, and implementation of SOPs and processes • Perform other duties as assigned

🎯 Exigences

• Bachelor’s degree or relevant experience • Preferred experience in the healthcare industry and FDA-regulated environment • Understanding of basic FDA and EMA regulations, ICH guidelines, GCP, and GMP • Experience with clinical logistics and pharmaceutical supply chain systems • Experience managing outsourced drug logistics, including warehousing, transportation, customs clearance, and invoicing • Familiarity with domestic and international logistics and transport of biologic material, including IATA, ICAO, ADR, DOT, and WHO requirements • Excellent interpersonal and collaboration skills • Ability to work independently and collaboratively to accomplish primary objectives • Strong analytical skills to develop solutions to complex problems • Organizational skills and ability to multitask and prioritize activities • Ability to support or lead vendor management efforts • Strong work ethic, ability to drive change, and passion for helping others • Must be authorized to work in the U.S. • East Coast-based candidates preferred • Willingness to eventually support EU operations

🏖️ Avantages

• Remote work 100% of the time • Collaborative environment • Opportunity to work with talented people

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