
1001 - 5000 employés
🏥 Santé
💼 Conseil
📦 Logistique
Healthcare • Consulting • Logistics
Worldwide Clinical Trials est une organisation mondiale de recherche contractuelle (CRO) qui offre des services complets d'essais cliniques. Ils se spécialisent dans le soutien aux études dans divers domaines thérapeutiques tels que l'oncologie, la cardiologie et les maladies rares. Avec plus de 30 ans d'expérience, Worldwide Clinical Trials met l'accent sur un soutien personnalisé et des solutions sur mesure tout au long du cycle de développement des médicaments. Leurs services incluent la surveillance clinique, la gestion des données, le recrutement de patients et le conseil réglementaire, garantissant précision et attention sur-mesure pour chaque essai clinique.
🕒 il y a 18 jours
🐊 Florida, Nevada, +6 états de plus – Distant
💵 $70 500 - $139 500 / an
⏰ Temps Plein
🟢 Junior
🟡 Intermédiaire
💻 Ingénieur Solutions
🦅 Parrain de Visa H1B
👻 Score fantôme 0%
🗣️🇺🇸🇬🇧 Anglais requis
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1001 - 5000 employés
🏥 Santé
💼 Conseil
📦 Logistique
Healthcare • Consulting • Logistics
Worldwide Clinical Trials est une organisation mondiale de recherche contractuelle (CRO) qui offre des services complets d'essais cliniques. Ils se spécialisent dans le soutien aux études dans divers domaines thérapeutiques tels que l'oncologie, la cardiologie et les maladies rares. Avec plus de 30 ans d'expérience, Worldwide Clinical Trials met l'accent sur un soutien personnalisé et des solutions sur mesure tout au long du cycle de développement des médicaments. Leurs services incluent la surveillance clinique, la gestion des données, le recrutement de patients et le conseil réglementaire, garantissant précision et attention sur-mesure pour chaque essai clinique.
• Ensure pricing tools and production systems meet service level agreements by analyzing and resolving issues and implementing bug fixes • Design and implement software solutions, including data integration, automation, monitoring, and reporting • Lead technical execution of pricing tool modernization and consolidation for the REBOOT Pricing Strategy • Support project managers and other functions with specifications, plans, reports, and technical documentation • Translate User Requirements Specifications into technical designs • Prepare, review, and approve design and integration documentation for pricing systems and cross-functional data flows • Perform coding, configuration, code reviews, and unit testing • Complete Traceability Matrices and maintain audit-ready documentation • Coordinate integration processes between systems and vendors such as Salesforce and Certinia • Determine requirements, configuration needs, and acceptance criteria with technical and non-technical project teams • Write and execute scripts • Support Test Analysts and business users during testing and quality review • Perform QC checks of manual data edits to protect data integrity • Investigate and resolve issues affecting pricing tools and automated workflows • Document activities according to SOPs and client requirements • Provide support and training to users of the in-house pricing tool • Identify and implement process improvements that reduce manual effort, increase scalability, and strengthen governance and auditability • Perform other duties as assigned
• Educated to degree level in a relevant discipline (e.g., Computer Science, Information Systems, Finance, Analytics) or able to demonstrate equivalent experience • Sound working knowledge of one or more of: .NET Framework, C#, Visual Studio, advanced VBA, relational databases and SQL, Power Query, Microsoft Power Platform, API/bus integration technologies, Java and Java Server technologies, UNIX, C, or C++ • Demonstrated experience developing and automating pricing, financial, or business process tools using advanced Excel, VBA, SQL, and data transformation techniques • 2+ years' experience in a combination of Contract Research Organization (CRO) experience, IRT study delivery, clinical systems development, or comparable business systems/pricing technology development desired • Familiarity with clinical trials, patient safety, data integrity, and associated regulations • Ability to communicate concisely and effectively in both written and spoken English • Proficient in common office software, with advanced Microsoft Excel capability • Able to work independently or within a multi-disciplinary team • High attention to detail • Able to adapt to new technologies, concepts, and processes, make improvements, and solve problems
• Competitive benefits package depending on location • Inclusive and equitable workplace • Transparent compensation and pay equity
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🦅 Parrain de Visa H1B
🗣️🇺🇸🇬🇧 Anglais requis
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