MLR Vault Technician

🕒 June 16

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Parexel

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Responsible for completion of tasks in the MLR Platform of Veeva Vault PromoMats and Veeva Vault Medical • Creating Placeholders, Uploading versions, Reference Linking, Anchoring & Linking • Monitoring the Workflows/Task completion • Work in an international and cross-functional environment, following global and local guidelines • Work closely with internal and external stakeholders to ensure high asset quality • Create new placeholders, Upload MLR content, Upload Reference Documents • Send Reference Documents for QC, Link Reference Documents • Start and monitor QC workflows, Communicate with users about task progress

🎯 Requirements

• Relevant Scientific, Medical or Data Analysis background preferred • Relevant experience with Veeva Vault PromoMats or Medcomms preferred • Strong attention to detail and accuracy, ability to manage and prioritize multiple, detailed activities • Fluent in oral and written English • Ability to work within a team or independently • Values teamwork, collaboration, diversity and inclusion, and innovation. • Prior experience working in content creation for Biotech/Pharma preferred. • Prior experience with the Pharmaceutical Content Review process and/or Veeva Vault preferred.

🏖️ Benefits

• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development