Reg. Information Management & Data Office Apprenticeship
Job PurposeĀ
The information (data and documents) managed by Regulatory Information Management & Data Office is critical to patientĀ
safety, regulatory compliance and effective business operations. Regulatory Information Management & Data Office areĀ
responsible for the accurate encoding of GSK product (Pharmaceuticals and Vaccines) registration information and maintainingĀ
regulatory records to a high standard appropriate to support critical regulated processes including Pharmacovigilance and GMP
compliant product supply. This data also supports the efficient operational management of the Regulatory function, worldwide.Ā
The role provides operational support to RIMS end-users.Ā
Key Responsibilities: Ā Describe the key deliverables to be achieved by the post holder and the ongoingĀ
responsibilities of the role. Ā
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⢠Accurate completion of routine data maintenance tasks to agreed scheduleĀ
⢠Ensure own work is compliant with data standards and defined proceduresĀ
⢠Ensure defined quality control procedures are followed and appropriate actions taken following any issues identified duringĀ
routine quality monitoring activitiesĀ
⢠Routine/ ad-hoc extraction and transformation of raw data from various Regulatory Information Management SystemsĀ
(RIMS) for KPI generation in the context of data quality improvement and performance monitoringĀ
⢠Maintain knowledge of GSK standards and procedures associated with RIMS and contribute to the definition of new andĀ
revised procedures to improve quality and effectivenessĀ
⢠Indexing, abstracting and quality assurance of Health Authority (HA) submissions and associated correspondence intoĀ
established regulatory document management system(s). Ā
⢠Support customer requests, as needed, by conducting specific searches for proprietary regulatory information using on-lineĀ
databases.Ā
⢠Maintain knowledge of GSK standards and procedures associated with registration data management and contribute to theĀ
definition of new and revised procedures to improve quality and effectivenessĀ
⢠Working on projects as required in response to internal and external customer requests.Ā
⢠Trouble shoot problems when required and propose appropriate solutionsĀ
⢠Supporting Legal and Business Development project work for document discovery, in-licensing, and out-licensing initiatives.Ā
⢠GQA Activities (where applicable)Ā
o Accurate completion of routine data maintenance tasks to agreed scheduleĀ
o Ensure own work is compliant with data standards and defined proceduresĀ
o Ensure defined quality control procedures are followedĀ
o Ensure CQA and PVQA data is entered accurately into the audit management system and within the requiredĀ
timelines working on Special projects as required in response to internal and external customer requests.
Skills
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Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases ā to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so weāre committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Inclusion at GSK:
As an employer committed to Inclusion, we encourage you to reach out if you need any adjustments during the recruitment process.
Please contact our Recruitment Team at IN.recruitment-adjustments@gsk.com to discuss your needs.
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