.Regulatory Specialist, RIM (Temporary 1.5 years)The purpose of this role is to ensure that GSK product (Pharmaceuticals and Vaccines) registration information and regulatory records are maintained to a 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. The role provides operational support to RIMS (Regulatory Information Management) end-users.The information managed is the formal record of GSK regulatory activity (documents and data) and is critical to patient safety, regulatory compliance and effective business operations. The post holder is accountable for the quality and accuracy of their own work and for the support of the large number of other users across GSK.Your Responsibilities: This role gives YOU the opportunity to lead key activities to progress YOUR career, the main of these are:Accurate completion of routine data maintenance tasks to agreed schedule.Ensure own work is compliant with data standards and defined procedures.Ensure defined quality control procedures are followed.Capable of performing routine data extraction from RIMS (Regulatory Information Management) to support KPI generation.Maintain knowledge of GSK standards and procedures associated with RIMS (Regulatory Information Management) and contribute to the definition of new and revised procedures to improve quality and effectiveness.Indexing, abstracting and quality assurance of US/UK submissions and associated correspondence into established regulatory document management system(s).Supporting Legal and Business Development project work for document discovery, in-licensing, and out-licensing initiatives.Support customer requests, as needed, by conducting specific searches for proprietary regulatory information using on-line databases.Working on Special projects as required in response to internal and external customer requests.Support for IT related activities.Why you?Basic Qualifications: We are looking for professionals with these characteristics to achieve our goals:Bachelor's degree in biological or healthcare science qualification or experience within Regulatory Affairs in the Drug development environment.0-3 years' experience in Regulatory Affairs Data Management (in pharmaceutical industry, life sciences research or regulatory).Advanced English.Availability to work in office 2 days per week.Demonstrated ability to proactively manage workload, timelines and identify priorities. Build relationships with relevant internal functions.Proven ability to work on multiple projects simultaneously.Preferred Qualifications: However, if you have the following, it would be a plus:Project Management.If you feel this is your next career move, please apply up to June 14th, 2023