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About the Job In Detail

Study Data Team Specialist

Posted on 
03-07-2023
Hertfordshire
Clinical Research
Good rate
Contract
Full-time
Job Category: 

Job Description

You will assist the team in charge of Clinical Trial label creation and approval within existing GMP computer systems. The role will entail carrying out GMP activities related to Clinical Study Data Entry and Approval with a strong emphasis on getting it right the first time and meeting defined supply chain lead-times. To ensure that business requirements are met, the role will necessitate the ability to collaborate across multiple departments. Execute pre-label creation activities efficiently to ensure the accuracy and compliance of GMP data within Global Packaging Operations. Supporting Global Packaging Operations teams in all aspects of Clinical Trial pack and label approval. In collaboration with key supply chain business partners, seek and support internal and broader process improvement opportunities. Principal Responsibilities: Include aspects of budget control, people management, technical activities, health and safety, GMP, and individual specific activities in your list of job activities. To ensure that data entry is accurate and completed in accordance with GMP guidelines. In charge of creating and approving data related to Clinical Labels. Capability to use relevant computer programmes, such as Excel and Word Multi-skills are expected, i.e. the ability to work in other areas when needed. Complies with applicable Standard Operating Procedures to ensure the accuracy of GMP activities. Understand the supply chain process to ensure timely and accurate delivery of information and documentation to the next node in the chain. Look for opportunities to develop and improve existing Data Entry for Label Creation processes. Competencies: Include breadth and depth across disciplines or functions; behaviours and field expertise Computer skills in the Microsoft Office suite of products are required. Excellent attention to detail. Understanding of clinical packaging and manufacturing terminology is required. Good Manufacturing Practices (GMPs) knowledge is preferred. Self-motivated, capable of managing own time and workload priorities Ability to identify and bring problems to the attention of the Team Leader as they arise. Effectively collaborates with others to meet deadlines, business goals, and objectives. Ability to collaborate across departments to achieve desired results for the organisation. #4364772

You will assist the team in charge of Clinical Trial label creation and approval within existing GMP computer systems.
The role will entail carrying out GMP activities related to Clinical Study Data Entry and Approval with a strong emphasis on getting it right the first time and meeting defined supply chain lead-times.
To ensure that business requirements are met, the role will necessitate the ability to collaborate across multiple departments.
Execute pre-label creation activities efficiently to ensure the accuracy and compliance of GMP data within Global Packaging Operations.
Supporting Global Packaging Operations teams in all aspects of Clinical Trial pack and label approval.
In collaboration with key supply chain business partners, seek and support internal and broader process improvement opportunities.
Principal Responsibilities:
Include aspects of budget control, people management, technical activities, health and safety, GMP, and individual specific activities in your list of job activities.
To ensure that data entry is accurate and completed in accordance with GMP guidelines.
In charge of creating and approving data related to Clinical Labels.
Capability to use relevant computer programmes, such as Excel and Word Multi-skills are expected, i.e.
the ability to work in other areas when needed.
Complies with applicable Standard Operating Procedures to ensure the accuracy of GMP activities.
Understand the supply chain process to ensure timely and accurate delivery of information and documentation to the next node in the chain.
Look for opportunities to develop and improve existing Data Entry for Label Creation processes.
Competencies:
Include breadth and depth across disciplines or functions;
behaviours and field expertise Computer skills in the Microsoft Office suite of products are required.
Excellent attention to detail.
Understanding of clinical packaging and manufacturing terminology is required.
Good Manufacturing Practices (GMPs) knowledge is preferred.
Self-motivated, capable of managing own time and workload priorities Ability to identify and bring problems to the attention of the Team Leader as they arise.
Effectively collaborates with others to meet deadlines, business goals, and objectives.
Ability to collaborate across departments to achieve desired results for the organisation.
#4364772

Additional Information

Vacancy Reference
4364772

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