Medical, Legal, Regulatory (MLR) Vault Technician

MLR Vault Technician

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

The 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. 

Experience Level

Mid Level