Excelya एक वैश्विक कॉन्ट्रैक्ट रिसर्च ऑर्गनाइज़ेशन (CRO) है, जो बायोटेक, फार्मास्यूटिकल और चिकित्सा उपकरण कंपनियों को स्वास्थ्य सेवा उत्पाद विकसित करने और उपलब्ध कराने में सहायता करता है। 28 देशों में संचालित यह कंपनी विभिन्न चिकित्सीय क्षेत्रों में पूर्ण-सेवा, फंक्शनल सर्विस प्रोवाइडर (FSP) और संसाधन समाधान प्रदान करती है। इसका सहयोगात्मक और लचीला दृष्टिकोण ग्राहकों को जीवन बदलने वाली चिकित्सा पद्धतियों को आगे बढ़ाने के लिए आवश्यक विशेषज्ञता और कार्यान्वयन क्षमता उपलब्ध कराता है।
Senior Clinical Project Manager - Hybrid France
Lead local pharmaceutical clinical trial delivery for Excelya, a European contract research organization. Coordinate regulatory compliance, investigational sites, vendors, recruitment, data quality, and collaboration with global study teams.
विवरण
- Manage local clinical trial activities from study start-up through close-out
- Deliver global study plans locally while meeting timelines and quality expectations
- Act as the primary contact for investigational sites and regional stakeholders
- Maintain compliance with local regulations, ICH-GCP, and internal standard operating procedures
- Coordinate submissions to competent authorities and ethics committees when needed
- Track regulatory milestones and oversee corrective actions
- Support site selection, activation, monitoring, and close-out with CRAs and vendors
- Manage local vendor relationships across logistics, laboratory, and CRO services
- Monitor recruitment, site performance, and operational metrics
- Partner with global study teams and medical, regulatory, and clinical operations functions
- Attend study meetings and report on local progress, issues, and outcomes
- Assist with risk mitigation and operational problem-solving
- Oversee data quality, query resolution, and documentation compliance
- Monitor KPIs, recruitment, timelines, and operational deliverables
- Support audit and inspection readiness activities
आवश्यकताएँ
- Background in clinical operations within a pharmaceutical company or CRO
- Experience working as a Clinical Project Manager, Study Manager, or in a comparable role
- Prior participation in interventional Phase II–IV trials is preferred
- Strong knowledge of ICH-GCP, regulatory requirements, and local clinical research practices
- Experience working with investigators, CROs, and cross-functional teams
- Well-developed organizational, operational, and communication abilities
- Able to prioritize and manage multiple responsibilities in a fast-moving setting
- Fluent written and spoken French and English
लाभ
- Build expertise through varied and engaging projects
- Work alongside recognized industry specialists
- Help advance scientific, operational, and human knowledge
- Join a workplace that recognizes individual strengths and supports initiative
- Develop professionally while contributing to a shared mission
- Be part of an organization focused on employee experience
- Work with an ambitious healthcare company and a 900-person team