Clinical Partnership Manager

About us
Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here.
At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.
Diversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.
Chiesi Research & DevelopmentOur R&D team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D project and portfolio management.  Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China).
Who we are looking forThis is what you will doWithin Global Clinical Operations and reporting to the Clinical Partnerships & Operations Excellence Lead, the Clinical Partnership Manager will play a key role in enabling, fostering and optimizing the governance and operational model of strategic partnerships with CROs, working closely with clinical study teams, category managers and other key stakeholders.
You will be responsible forDevelops and manages strong, trust-based partnerships with external stakeholders, particularly CROs, and by embedding excellence, agility, and innovation into the clinical delivery modelEnsures the technical maintenance, monitoring and continuous improvement of an effective operational and partnership model within GCOFosters a sustainable and future-proof vendor management approach aligned with Chiesi’s portfolio and long-term strategic visionDevelops and manages vendor partnership model and ensure appropriate governance to assure the highest quality delivery of clinical trialsCollaborates in vendor selection, onboarding and integration of digital platforms and services, collaborating with the involved internal parties (GICT, etc..)Maintains strong relationships with CROs/vendors to ensure a collaborative and productive partnershipLiases with internal and external stakeholders to leverage best practices, technology and expert knowledgeDefines Third-Party Vendors Governance, vendors panels and oversees setup activities, timelines and performance to ensure alignment with company SOPs, study protocols, and company objectivesPartners closely with Procurement to support preparation of Master Service Agreements/Service Level Agreements and related documentation and to ensure compliance with contractual agreementsDevelops and mantains collaborative relationships with external partners to enhance delivery capabilities and innovationCollaborates in the assessment and technical implementation of current and new processes/procedures within GCO, in light of the revision of GCO operational modelCollaborates with GCO/GCD leadership and workstreams to identify opportunities for sharing best practicesIdentifies process issues and develop resolutions to meet productivity, quality and internal and external stakeholder satisfaction goals and objectivesContributes in the identification of the best fitting technological infrastructure(s) to exploit the increasing external offer of solutionsPartners with study teams to prepare for and engage in interaction with strategic providers to ensure successful outcomes for studies (e.g. revision of RFP, change order requests)Partners with study teams to prepare for and engage in interaction with strategic providers to ensure studies success (e.g.participation to BDM, KOM and other applicable study level interactions)Partners with QA for vendor qualification and manteinanceFosters a culture of continuous improvement, setting high performance standards, focusing on exceeding objectivesYou will need to have8–10 years of relevant experience in Clinical Operations, with solid knowledge of clinical trial management and the different phases of clinical developmentAbility to navigate complexity and manage multiple priorities while maintaining strong attention to detailProven exp