What are the responsibilities and job description for the Document Control Records Management - Specialist - Document Controls (Entry Level) position at TalentBurst, an Inc 5000 company?
Document Control Records Management - Specialist - Document Controls (Entry Level)
100 % Remote
6 Months Contract
Job Description: This position is 100% remote with no preference to region or time zone. Please ensure that the candidate city and state is listed on resume
Position Summary: The Document Controls Specialist for Leica Biosystems is responsible for maintaining data integrity, supporting content management system migration, enhancing regulatory compliance, and driving cross-system consistency.
This position is part of the Global Regulatory & Clinical Affairs team and will be remote. At Leica Biosystems, our vision is to advance cancer diagnostics and improve lives.
You will be a part of the Regulatory & Clinical Affairs Operations team and report to Senior Project Manager, Regulatory & Clinical Affairs Operations responsible for collaborating with Global Marketing and Regulatory Affairs teams to drive cohesive project execution. If you thrive in a cross functional, detail oriented role and want to work to build a world-class Marketing and Regulatory Affairs organization — read on.
In this role, you will have the opportunity to drive operational efficiency, compliance, and system readiness through the following:
Job #: 25-33243
100 % Remote
6 Months Contract
Job Description: This position is 100% remote with no preference to region or time zone. Please ensure that the candidate city and state is listed on resume
Position Summary: The Document Controls Specialist for Leica Biosystems is responsible for maintaining data integrity, supporting content management system migration, enhancing regulatory compliance, and driving cross-system consistency.
This position is part of the Global Regulatory & Clinical Affairs team and will be remote. At Leica Biosystems, our vision is to advance cancer diagnostics and improve lives.
You will be a part of the Regulatory & Clinical Affairs Operations team and report to Senior Project Manager, Regulatory & Clinical Affairs Operations responsible for collaborating with Global Marketing and Regulatory Affairs teams to drive cohesive project execution. If you thrive in a cross functional, detail oriented role and want to work to build a world-class Marketing and Regulatory Affairs organization — read on.
In this role, you will have the opportunity to drive operational efficiency, compliance, and system readiness through the following:
- Support current process of archiving marketing materials in content management system and conducting periodic reviews
- Assessing and aligning current content management platforms
- Assist Senior Project Manager content management system transition, including c hange management
- Cross functionally collaborates with global marketing, regulatory affairs, and other relevant stakeholders
- Bachelor's degree
- 3 years of relevant experience
- Proficiency in Microsoft Office applications, experience in content management preferred
- Ability to travel – 5%
- Regulatory Affairs
- Marketing
- Project Management
- Working with global, cross-functional teams
Job #: 25-33243
