Project Manager

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🕒 vor 5 Monaten

🌐 Vereinigtes Königreich, Kroatien – Remote

🇬🇧 Vereinigtes Königreich – Remote 🇭🇷 Kroatien – Remote

⏰ Vollzeit

🟡 Mittelstufe

🟠 Senior

👷‍♀️ Projektmanager

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Medable

WebsiteLinkedInAlle Stellen

51 - 200 Mitarbeiter

🏥 Gesundheitswesen

💼 Beratung

📦 Logistik

💰 €300.000 Seed Round - MedAble im 2015-03

Healthcare • Consulting • Logistics

Medable ist ein SaaS-Unternehmen, das eine einheitliche, cloud-unabhängige Plattform für dezentrale klinische Studien (DCT) bereitstellt, die von Pharma-Sponsoren, CROs und Forschungsstandorten genutzt wird, um klinische Forschung effizienter zu gestalten und zu beschleunigen. Die Lösungen umfassen eCOA/ePRO, eConsent, Fernüberwachung, vernetzte Sensoren und KI-gesteuerte Werkzeuge (Agent Studio und mehrere KI-Agenten), um Prozesse der elektronischen Prüfakte, Standortabläufe und die Erfassung von Teilnehmerdaten zu automatisieren. Medable legt Wert auf schnellen Studienaufbau, globale Skalierbarkeit, Integrationen und patientenzentriertes Design, um die Zeit bis zum Start zu verkürzen und die Effizienz der Studien und die Datenqualität zu verbessern.

Beschreibung

• Manage the initial deployment lifecycle of the Medable Solution spanning project kick-off through go-live and system localization. • Collaborate with solution design teams to ensure a comprehensive understanding of trial-specific requirements. • Manages project scope, timelines and financial oversight, including submitting and approving timecards (as applicable) and ensuring the project remains within budget. • Ensure the design teams align the System Specifications to the clinical trial protocols and detailed schedules of assessments within the scope of the study contract • Develop adaptive project plans seamlessly incorporating evolving client needs and trial requirements without disrupting project momentum. • Implement robust change management practices by proactively identifying, evaluating, and integrating change requests. • Educate clients and internal teams on software capabilities, customization options, and best practices for integration into clinical trial processes. • Provide expert oversight for ongoing projects requiring system enhancements or modifications. • Take decisive action to realign project deliverables when requirements or priorities shift. • Ensure continuous progress and maintain project integrity. • Facilitate the translation of client requirements into fully functional software solutions. • Develop and execute comprehensive, detailed project plans that strategically outline timelines, critical milestones, and optimal resource allocation. • Support successful software implementation through coordinated planning and execution. • Build and maintain strong, collaborative relationships with clients through transparent and consistent communication serving as the primary point of contact for all project updates, issue resolution, and ongoing support. • Proactively identify potential risks and challenges throughout the project lifecycle. • Develop strategic mitigation strategies that anticipate potential obstacles. • Create comprehensive guidance materials and conduct knowledge transfer sessions for the Study Conduct team. • Collaborate extensively with cross-functional teams including developers, product managers, and clinical trial experts. • Facilitate cohesive communication to ensure delivery of solutions that meet complex client and regulatory expectations. • Conduct rigorous analysis of project outcomes to identify opportunities for methodological refinement and process improvement. • Drive continuous organizational enhancement through data-driven insights and recommendations.

🎯 Anforderungen

• Minimum of 6 years of experience or an equivalent combination of related education and experience. • Proven experience in managing full lifecycle software implementation projects with a track record of supporting solution design and delivery tailored to specific client requirements. • Advanced proficiency in change management showcasing the ability to handle complex change requests and effectively coordinate cross-functional teams with updated project objectives. • Extensive experience supporting in-flight projects requiring adaptive approaches or enhanced oversight. • Comprehensive understanding of clinical trial domains, specifically: eCOA (electronic Clinical Outcome Assessments) ePRO EDC DCT • Strong knowledge of clinical trial data management processes and regulatory compliance frameworks.

🏖️ Vorteile

• Flexible Work • Competitive base salaries • Annual performance-based bonus • Stock options for employees, aligning personal achievements to Medable's success • Health and insurance coverage • Wellness program (Mental, Physical and Financial) • Peer-to-peer recognition program, celebrating achievements and milestones • Volunteer time off to support causes you care about