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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.
Job Responsibility
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
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, 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
Nice to have
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