
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
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10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
• Manage courseware development including course design, publishing, testing and deployment • Provide technical, instructional design and operational management for programs and be accountable for meeting project commitments • Communicate and ensure a global understanding of training strategy and goals • Manage deliverables according to endorsed plans and timelines across multi-functional teams including course design, development and deployment • Partner with associated business line and Subject Matter Experts (SMEs) to proactively identify training needs and development and deployment of training programs • Advise on processes, monitor activities related to compliance oversight of training programs; ensure programs and projects are evaluated for effectiveness and customer satisfaction • Development of metrics and performance measures, reporting and analysis to meet business needs, and regulatory requirements • Ensure compliance to training and education regulatory requirements and consistent implementation of best practices, standards, and training globally to support inspection readiness • Serve as a role model and promote learner-centered approaches and methodologies
• Demonstrated knowledge of adult learning principles, experience design • Familiarity of the business of Clinical Research & Development, Pharmacovigilance, and/or Regulatory in the pharmaceutical industry • Demonstrated ability to manage multiple projects concurrently • Some prior experience in monitoring adherence to compliance-based training programs • Proficiency in Microsoft Office, Articulate suite, and at least one of the following: Adobe, Vyond, Camtasia • Minimum of 1 year of pharmaceutical industry with focus on pharmacovigilance, regulatory and or clinical development • Minimum of 5 years’ experience designing, developing, and delivering learning solutions
• Health insurance • 401(k) matching • Flexible work hours • Paid time off • Professional development opportunities
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