Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
MLR Vault Technician
Job ID R0000039691 , IndiaThe MLR Technical Reviewer will be responsible for completion of tasks in the MLR Platform of Veeva Vault PromoMats and Veeva Vault Medical, the tasks will be related to the role of Content Administrator, i.e. Creating Placeholders, Uploading versions, Reference Linking, Anchoring & Linking, monitoring the Workflows/Task completion.
The MLR Technical Reviewer will work in an international and cross-functional environment, following global and local guidelines and working closely with internal and external stakeholders to ensure the highest quality for assets and gathering data on asset quality and agency performance.
- Create new placeholders, based on relevant Metadata & guidance provided
- Uploading new MLR content, based on relevant Metadata & guidance provided
- Uploading new Reference Documents and sending them for QC, based on relevant information & guidance provided
- Reference Document linking, based on relevant information & guidance provided
- Anchoring & Linking, based on relevant information & guidance provided
- Starting QC workflows, based on relevant information & guidance provided
- Monitoring MLR workflows, based on relevant information & guidance provided
- Communicating with users or stakeholders to inform about task progress or completion
Skills:
- 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, results-orientated with fast and focused execution.
- Good communication, coordination and time management skills.
- Fluent in oral and written English
- Ability to work within a team or across multiple teams (including remotely) as well as independently.
- Values teamwork and collaboration, diversity and inclusion, and innovation.
- Prior experience working in content creation for Biotech/Pharma, would be advantageous.
- Prior experience with the Pharmaceutical Content Review process and/or Veeva Vault would be advantageous.
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