
1001 - 5000 funcionários
🧬 Biotecnologia
💊 Farmacêutico
🔬 Ciência
Biotechnology • Pharmaceuticals • Science
A Allucent é um parceiro de referência para empresas de biotech de pequeno e médio porte, oferecendo soluções inovadoras em assuntos regulatórios e desenvolvimento clínico. Com mais de 30 anos de experiência, a Allucent é especializada em expertise terapêutica, farmacologia clínica, estratégia regulatória, segurança de medicamentos e nos processos de farmacovigilância necessários para levar novas terapias ao mercado. Seus serviços abrangentes abordam desafios desde a descoberta de fármacos em fases iniciais até os ensaios clínicos e a vigilância pós-comercialização, apoiando diversas áreas terapêuticas, como oncologia, doenças infecciosas, neurologia, doenças autoimunes e doenças raras. O compromisso da Allucent em fomentar ciência de ponta ajuda as empresas de biotech a navegar pelas complexidades do desenvolvimento de medicamentos de forma eficiente e eficaz.
🕒 Maio 22
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

1001 - 5000 funcionários
🧬 Biotecnologia
💊 Farmacêutico
🔬 Ciência
Biotechnology • Pharmaceuticals • Science
A Allucent é um parceiro de referência para empresas de biotech de pequeno e médio porte, oferecendo soluções inovadoras em assuntos regulatórios e desenvolvimento clínico. Com mais de 30 anos de experiência, a Allucent é especializada em expertise terapêutica, farmacologia clínica, estratégia regulatória, segurança de medicamentos e nos processos de farmacovigilância necessários para levar novas terapias ao mercado. Seus serviços abrangentes abordam desafios desde a descoberta de fármacos em fases iniciais até os ensaios clínicos e a vigilância pós-comercialização, apoiando diversas áreas terapêuticas, como oncologia, doenças infecciosas, neurologia, doenças autoimunes e doenças raras. O compromisso da Allucent em fomentar ciência de ponta ajuda as empresas de biotech a navegar pelas complexidades do desenvolvimento de medicamentos de forma eficiente e eficaz.
• Responsible for overall quality and management of the delivery clinical trial projects and programs • Manages complex, cross-functional resource requirements in line with budgeted, time, scope, and quality expectations for project delivery • Oversees budgets and ensuring correct financial forecasting, planning, invoicing and timely implementation of out of scope activities • Reviews and approves content and costing of proposals • Ensures effective risk management across the project delivery lifecycle • Negotiates and influences internal and external team members in a professional manner and with successful outcomes • Effectively solves problems with projects teams by applying strategic thinking and conflict resolution skills • Balances multiple competing priorities, with effective and efficient resource utilization across projects and programs • Serves as key contact for assigned clients on delivery of scope, customer satisfaction on services and capabilities and the assessment of client needs • Shows knowledge of and insight into general business principles and practices, and is able to balance business priorities • Demonstrates a growth mindset, and approaches complex challenges with creativity and flexibility • Leads by example and encourages team members to develop strong solutions for clinical trial delivery • Supports the recruitment and interviewing of new employees • Responsible for supervision of project staff and communication with functional managers, including performance feedback • 10% of Business travel is required for this position, including possible international travel
• Minimum Bachelor’s degree in life science, healthcare and/or business degree; Master’s degree or greater preferred • Minimum 7 years of relevant work experience • Minimum 7 years of experience in drug development and/or clinical research • Extensive clinical project management experience, with at least 5 years of clinical project management experience • Preference for candidates with CRA experience • Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable (local) regulatory requirements • Strong financial acumen, administrative excellence and analytical skills • Experience managing global clinical trials • Excellent written and verbal communication, planning, critical thinking and organizational skills, including command of English language • Proficiency with various applications including but not limited to Microsoft Word, Excel, and PowerPoint required • Clinical trial delivery process expertise • Strong general administrative skills and experience • Outgoing and client focused • Proactive and solution oriented • Strong presentation and networking capabilities • Experience applying a data driven approach to drive clinical trial delivery solutions
• Comprehensive benefits package per location • Competitive salaries per location • Departmental Study/Training Budget for furthering professional development • Flexible Working hours (within reason) • Opportunity for remote/hybrid* working depending on location • Leadership and mentoring opportunities • Participation in our Buddy Program as a new or existing employee • Internal growth opportunities and career progression • Financially rewarding internal employee referral program • Access to online soft-skills and technical training via GoodHabitz and internal platforms
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