Site Contracts Lead

**Site Contracts Lead, Clinical Research** **Hybrid Role - Montreal, QC** **50% in office/50% remote** As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries. Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise. **Did you know?** **Why settle for one thing when you can have everything?** Labcorp Drug Development gives you the best two for one opportunity for career growth. Who doesn’t want twice the perks - working at one of the largest FSP CROs—and partnering with one sponsor with a dedicated therapeutic focus. Our Energizing Purpose, Exceptional People and Extraordinary Potential combined with collaborative and proactive teams offer a great place for you to continue honing your therapeutic skills and growing and excelling in new exciting research. Our reach is global - extending to 60+ countries making us one of the largest FSP CROs. So, no matter where you are located on the globe, we have an FSP opportunity for you. **Responsibilities** - Responsible for adherence to standard operating procedures (SOPs). - Provide knowledgeable single point of service to study teams related to study budgets and contracts. - Manages the end-to-end process for executing Clinical Trial Agreements with investigator sites. - Prepares, negotiates and executes Master Agreements with institutions. - Develop and maintain template language in collaboration with legal for all contract types, including maintenance of associated back-up language. - Prepares study / site level grant budgets. - Perform the following, with occasional guidance from line management or more experienced colleagues: daily tracking, negotiation and approval of Site Agreements and Site Agreement templates (as applicable) for clinical study teams; timely updating of the departmental Site Agreement Management System ("SAMS") or any other system required for use on a particular study. - Identify and escalate issues (as defined in departmental processes) that must be escalated to appropriate colleague for review. - Manage assigned studies with careful compliance with internal processes and procedures, or otherwise according to specified Sponsor requirements. - Drafts, negotiates, reviews, and processes contracts in a commercially reasonably manner that protects Labcorp's fundamental interests and in accordance with departmental practices and policies. - Produces and negotiates contracts that accurately reflect Labcorp Drug Development's obligations or rights and understandings with third parties. **Requirements**: - Bilingual English/French - Bachelor's degree required preferably within life sciences or equivalent. - 2 or more years’ experience negotiating legal and/or financial agreements, preferably in pharmaceutical industry clinical trials or years of industry related experience in clinical operations. - Working knowledge of clinical trial start-ups and finance cycles including knowledge of site needs and perspective. - Strong organization and time management skills and ability to effectively manage multiple competing priorities. - Strong communication skills with a strong customer focus, able to manage both internal and external clients at all organizational levels. - Strong negotiation and interpersonal skills including strong conflict resolution skills. **Great Benefits at Labcorp**: - Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: - Medical - Dental - Vision - Life, STD/LTD - 401(K) - ESPP - Paid time off (PTO) or Flexible time off (FTO) - Company bonus where applicable **Labcorp is proud to be an Equal Opportunity Employer**: As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. For more information about how we collect and store your personal data, please see our Privacy Statement.