Senior Business Analyst

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • 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.

📋 Description

• Analyze complex business processes across clinical research functions • Gather and translate stakeholder requirements into actionable documentation • Develop use cases, user stories, and functional specifications • Map current-state workflows and design future-state processes • Recommend process standardization and automation opportunities • Perform cost-benefit analyses and measure implemented improvements • Collaborate with technical teams on solution design and system implementations • Support test-plan and test-case development and validate implemented solutions • Develop training materials and end-user support documentation • Lead business analysis activities for medium- to large-scale projects • Manage project scope, deliverables, work plans, timelines, and requirements-related risks • Build stakeholder relationships and facilitate communication between business and technology teams • Present findings and recommendations to stakeholders • Mentor junior business analysts and share best practices • Monitor clinical research industry trends and regulatory changes and identify innovation opportunities

🎯 Requirements

• 5 to 7 years of business analysis experience, including at least 3 years in clinical research or the pharmaceutical industry • Experience leading requirements-gathering and process-improvement initiatives • Strong understanding of clinical trial processes and workflows • Experience with clinical systems implementation and configuration, including EDC, CTMS, and eTMF • Knowledge of clinical research regulatory requirements, including GCP, ICH, FDA, and EMA • Experience with Agile and traditional software development methodologies • Bachelor's degree in business administration, information systems, life sciences, or a related field • Advanced analytical and problem-solving skills • Expertise in business process analysis, requirements management, and process improvement methodologies • Proficiency with JIRA, Confluence, and Visio • Familiarity with BPMN, UML, and flowcharts • Exceptional written and verbal communication, facilitation, and presentation skills • Leadership capabilities in mentoring, project coordination, decision-making, and influencing without authority • Experience in clinical research, pharmaceutical, or other regulated environments • Patient-focused mindset, attention to detail, and commitment to regulatory compliance and quality standards • Preferred: CBAP, IIBA, or PMI-PBA certification • Preferred: Lean or Six Sigma training • Preferred: experience implementing or optimizing clinical data management processes • Preferred: experience leading cross-functional teams and facilitating decision-making

🏖️ Benefits

• Flexibility • Growth opportunities • Continuous learning opportunities • Career paths and opportunities to expand skills across clinical research operations and technology integration