What are the responsibilities and job description for the Label Project Coordinator II - Clinical Supply Chain position at Kelly Science, Engineering, Technology & Telecom?
About the Role
As a Label Project Coordinator II - Clinical Supply Chain at Kelly Science, Engineering, Technology & Telecom, you will play a critical role in ensuring the seamless execution of clinical trials. Your primary responsibility will be to translate clinical trial protocols and packaging specifications into clinical label generation software.
- You will design clinical supplies trial labels for primary, secondary, and auxiliary packaging applications within the label systems.
- Interpret randomization schemes and input them into label software systems to verify correct labels are produced according to cGMPs.
Key Responsibilities:
- Ensure all clinical supplies and associated documentation are processed according to GMPs/GDP's and safety requirements.
- Liaise with country-level clinical operations personnel or regulatory affairs to address questions, revise translations, update regulatory requirements, etc.
Requirements:
- Bachelor's degree in a relevant field or equivalent combination of education and 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.
This is an excellent opportunity for a detail-oriented and organized individual to join our team and contribute to the success of our clients.
