Global Study Management Associate

🕒 Outubro 28

🇺🇸 Estados Unidos – Remoto (EUA)

💵 $72.800 - $97.800 / ano

⏰ Tempo Integral

🟢 Júnior

🟡 Pleno

👻 Score fantasma 1%

O que significa: a chance de ninguém estar realmente contratando para esta vaga.Como ler: 60% ou mais significa que achamos que é uma vaga fantasma. Pontuações mais baixas preocupam menos.Por que essa pontuação:

• Aberta há 15 dias.
• As vagas desta empresa costumam ser preenchidas em 41 dias.

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BeOne Medicines

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 2010

🧬 Biotecnologia

🏥 Saúde

💊 Farmacêutico

Biotechnology • Healthcare • Pharmaceuticals

A BeOne Medicines é uma empresa global de oncologia, com sede na Suíça, que descobre e desenvolve tratamentos inovadores mais acessíveis e com maior disponibilidade para pacientes com câncer em todo o mundo. Com um portfólio que abrange hematologia e tumores sólidos, a BeOne está acelerando o desenvolvimento de seu diversificado pipeline de novas terapias por meio de capacidades internas e colaborações. Com uma equipe global em crescimento, formada por mais de 11.000 colaboradores presentes em seis continentes, a empresa está comprometida em melhorar radicalmente o acesso a medicamentos para muito mais pacientes que deles precisam.

Descrição

• Support the Global Clinical Study Manager in global study delivery and execution of delegated clinical study components within quality, timeline, and budget expectations • Support alignment of study goals with clinical operations objectives • Support organization and logistics for cross-functional Clinical Study Team meetings • Collaborate with Global Clinical Study Manager, Regional Clinical Trial Management Associates, and global and regional stakeholders • Create and maintain study-level SharePoint resources and CST distribution lists • Set up studies in systems such as eTMF and CTMS and keep study information current • Manage study-system access and user accounts throughout the study lifecycle • Support development of study plans and organization of investigator meetings • Support site feasibility assessments • Track study deliverables including screening, enrollment, biological samples, images, data flow, and protocol deviations • Prepare management metrics and updates • Support study newsletters and study-conduct correspondence • Support study-level TMF creation, maintenance, document review, and quality control • Support study drug forecasts and supply activities • Support data cleaning and follow-up of outstanding information • Support planning and execution of Clinical Study Reports • Identify operational risks and issues and recommend solutions • Suggest improvements to enhance efficiency and quality • Support vendor selection and setup for global outsourced activities • Support study budget management, purchase-order setup, and invoice tracking

🎯 Requisitos

• Bachelor or higher degree in a scientific or healthcare discipline required; higher degree preferred • Exceptions might be made for candidates with relevant clinical operations experience • 1 or more years of experience in clinical research within Biotech, Pharma or CRO industry • Knowledge of clinical operations methodologies and understanding of operational aspects of clinical study processes • Knowledge of clinical study operations, including interpretation and implementation of regulatory and ICH-GCP guidelines • Proficiency in MS Office Suite, including Excel, PowerPoint and Project • Limited travel might be required

🏖️ Benefícios

• Annual bonus plan eligibility for non-commercial roles • Discretionary equity awards • Employee Stock Purchase Plan • Medical insurance • Dental insurance • Vision insurance • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness

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