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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.
Medical Scientific Associate - FUSE Superuser - FSP
Job ID R0000035050 , ArgentinaPosition Overview
The Medical Scientific Associate is responsible for system governance, quality assurance, and cross-collaboration support for the FUSE Digital Asset Management (DAM) system. This role serves as a critical link between Global/International workflows, ensuring system integrity while providing advanced troubleshooting and problem-solving capabilities as a FUSE Superuser.
Key Responsibilities
System Oversight and Enhancement
Identify system issues and global enhancements through rigorous testing and QA of Global/International workflows
Serve as primary contact for cross-collaboration with the FUSE enterprise team during super user calls
Support the Global FUSE Lead with expanded system access and permissions
Troubleshoot and resolve various system issues by accessing advanced backend capabilities
Compliance and Governance
Ensure Global Content Owners adhere to post-usage country requirements
Review and manage dormant accounts, including sending communications and revoking access when necessary
Monitor in-process assets that remain unfinished and take appropriate action
Track and document deviations when SOPs and processes are not followed
Access Management
Approve/reject User Access Management (UAM) application requests
Verify training criteria completion and correct role profile selection
Maintain agency profiles with regular updates
Approve brand/therapeutic area access for the FUSE DAM
Qualifications
Experience
1-2 years' experience in pharmaceutical/biotech or advertising industry and/or digital marketing operations
Functional experience in a pharma or CRO environment in regulatory, medical, or marketing operations
FUSE system experience required
Knowledge and Skills
Working knowledge of compliance guidelines on advertising and promotion
Basic understanding of process optimization and asset creation
Proficiency in computer applications, including Microsoft Office and Adobe Acrobat
Organizational Skills
Ability to interact comfortably with all levels and departments of the organization, including senior leadership
Exceptional facilitation skills to drive consensus quickly in a progressive, change-intensive environment
Strong risk identification, mitigation, and management capabilities
Excellent project and process management skills
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