Senior Clinical Contracts Analyst - France - FSP

<p><b>When our values align, there's no limit to what we can achieve.</b><br/> <br/>At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.</p><p>Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.</p><p></p><p></p><p>Working as a Senior Clinical Contracts Analyst at Parexel offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global Biotechs and Pharma top 50, and we have an incredible pipeline of work.</p><p></p><p>Whether you see your future path in contracts analysis, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.</p><p></p><p>Our CCAs are valued members of our clinical studies teams, working from their home office base, supporting studies within their country or region. ‘Manageable’ is our mantra. Expect exciting professional challenges on inspiring studies, but with time for your outside life.</p><p></p><p><b>Purpose of the role</b></p><p><span>                                                                                                                         </span></p><p>Parexel supports clinical studies across the full range of oncology and non-oncology therapeutic areas, and we have longstanding partnerships with a vast client base.</p><p></p><p><span>Dedicated to one key sponsor</span>, the Senior Clinical Contract Analyst serves as a conduit between Clinical Operations and the Legal group for contract requests including Confidentiality Agreements, Clinical Trial Agreements (CTAs), Ancillary Services Agreements, Consultant Agreements, and other clinical contracts.</p><p></p><p><b>What you’ll be doing</b></p><ul><li><p>Manage Clinical Contract and Nondisclosure Agreement (NDA) process for Global trials</p></li><li><p>Serve as a conduit between Clinical Operations and the Legal group for contract requests including Confidentiality Agreements, Clinical Trial Agreements, Ancillary Services Agreements, Consultant Agreements, and other clinical contracts</p></li><li><p>Process all clinical contract requests and help facilitate early execution through the Contract Management System</p></li><li><p>Serve as primary contact for the Client during contract negotiation phase</p></li><li><p>Perform consistent quality audits of work output and document knowledge base as needed</p></li><li><p>Maintain contract tracking on SharePoint site and other systems used to manage contract and budget files</p></li></ul><p></p><p>Negotiate Clinical Site Contracts &amp; Budgets for Sites Managed by Sponsor:</p><ul><li><p>Manage and own the contract process through its lifecycle from initial template stage to fully negotiated contract</p></li><li><p>Work closely with study teams to develop country budget templates tailored for each study</p></li><li><p>Negotiate and manage consistent site budgets that will assist in early site activation</p></li><li><p>Ensure consistency in site payment schedules and terms to facilitate the payment system</p></li><li><p>Respond to queries related to contracts and budgets</p></li><li><p>Manage the contract escalation process to appropriate individuals, as needed</p></li><li><p>Establish good customer relations with sites starting with the primary point of contact for budgets and contracts</p></li><li><p>Analyze contract trends using available tools and assist with developing team metrics regarding contract timelines.</p></li></ul><p></p><p>For Sites Managed by a Clinical Research Organization (CRO):</p><ul><li><p>Review and approve the master Investigator Fee template developed by CRO for each study before distribution to sites</p></li><li><p>Manage the final execution of site clinical contracts handled by a CRO and track the contract process for each study with a CRO.</p></li><li><p>Serve as escalation point of contact for budget escalations from CRO.</p></li><li><p>Provide contract/budget comments to CRO on an as needed basis.</p></li><li><p>Respond to CRO queries for previously negotiated site contracts to ensure consistency with contract language and budget line items</p></li></ul><p></p><p>At Parexel we believe strongly in work/life balance we’ll take your well-being just as seriously as we do that of our patients.</p><p></p><p>To us, that’s what ‘working with heart’ is all about.</p><p></p><p><b>What you’ll need to join us as a Senior Clinical Contracts Analyst:</b></p><p></p><p>Skills and Education:</p><ul><li><p>Bachelor’s degree in Life Science, Business or equivalent. MBA preferred</p></li><li><p>Minimum four (4) years of global experience wor