What are the responsibilities and job description for the Clinical Label Generation Expert position at Kelly Science, Engineering, Technology & Telecom?
Responsibilities and Expectations
The Label Project Coordinator II will be responsible for managing the creation of clinical trial protocols and packaging specifications in clinical label generation software. This includes designing clinical supplies trial labels for primary, secondary, and auxiliary packaging applications within the label systems.
Main Accountabilities:
- Develop and implement effective processes for translating clinical trial protocols into clinical label generation software.
- Design and develop clinical supplies trial labels for primary, secondary, and auxiliary packaging applications.
- Work closely with country-level clinical operations personnel or regulatory affairs to ensure accurate and compliant translations.
- Collaborate with Clinical Supply Program Managers, Supply Planners, Quality, Pharmaceutical Sciences, or other stakeholders to achieve project goals.
Qualifications:
- BS/BA or appropriate combination of education and relevant practical experience.
- Working knowledge of Packaging Operations and related work centers.
- Proactive approach to work, identifying potential issues and bringing them to the attention of appropriate personnel for resolution.
- Strong attention to detail.
- Strong verbal and written communication skills.
- Strong organizational skills, ability to prioritize and ability to multi-task.
