
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
đ„ 36 minutes ago
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10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
âą Serve as the site contracts and budgets lead across assigned studies accountable for ensuring the timely, high quality and compliant execution of the site budget and contract negotiation process âą Collaborate with key stakeholders on the study team from early planning and throughout the contract lifecycle to prioritize, plan and execute in alignment with operational objectives âą Actively and regularly drive prioritization and progress on site contracts within the clinical trial working group âą Develop or oversee budget setup including study-specific parameters for assigned studies using industry tools and data sources âą Manage site contracting related issues efficiently and according to escalation pathways âą Communicate effectively internally and with external partners to ensure alignment and excellence in coordination of study start-up activities (i.e. SIV scheduling) âą Ensure that all relevant systems and trackers are accurate and timely with regard to the disposition of site budgets and contracts âą Apply standards to the site budgeting and contracting process across studies/programs âą Manage all changes to study scope ensuring timely implementation of amendments âą Lead site budget and contract process improvement initiatives, as required âą Manage against study-level KPIs and metrics for site budget and contract negotiation âą Train and mentor peers and stakeholders, as required
âą +5 years of site budget and contract experience âą Strong knowledge of site contracting practices and understanding of challenges âą Demonstrated understanding of clinical operations and study start-up âą Demonstrated experience with driving global site budget and contract strategies âą Familiar with common budget development and data tools (e.g. Grant Plan) âą Demonstrated understanding of regulatory and legal issues related to the conduct of clinical trials
âą Complies with required training curriculum âą Completes timesheets accurately as required âą Submits expense reports as required âą Updates CV as required âą Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements
Apply Nowđ July 3
Clinical Trial Manager focusing on project management for drug development at Syneos Health in Argentina. Responsible for clinical monitoring and patient safety oversight in clinical trials.