RIM Business Analyst / Project Manager

Teva Pharmaceuticals ,
Harlow, Essex
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RIM Business Analyst / Project Manager Date: Apr 24, 2020 Location: Harlow, GB, CM20 2FB Company: Teva Pharmaceuticals Who Are We? We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us. We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world. We are looking for a RIM Business Analyst / Project Manager to join the Global Regulatory Operations team in our office in Harlow, Essex. A Day in the Life of... + You will help develop and implement the Regulatory Affairs business data management and related business systems strategy to ensure that the Global Regulatory Affairs systems and data management processes continue to meet ongoing and emerging business needs. + You will provide the expert business analysis input required for the successful development of strategic system roadmaps and for the successful implementation of the projects required to ensure the delivery of the technology solutions required to support the GRA business and its partner functions. + You will provide RA Business Data Administration and Business System Ownership, including system and data related business change management, in support of the RA business process and data requirements, and compliant system usage. + You may partner with external pharmaceutical industry stakeholders and health authorities to influence outcomes relating to emerging requirements such as ISO IDMP and FMD etc. + You will help manage and deliver an in-house Centralised Data Service to GRA for the management of Teva registration data. This includes support for data integration and data integrity/enrichment initiatives to ensure compliant and reliable RA data for accurate reporting and business decisions making. Who we are looking for Are you.... + Fluent with Pharmaceutical Regulatory Affairs business processes? + Analytical, methodical and able to analyse data, process and external regulatory requirements? + Able to communicate to a high level through both verbal and written channels? + Able to demonstrate experience of leading cross-functional project teams and change projects? Do you have.... + A Degree or Masters in Life Sciences? + Experience with Parexel/Liquent's Insight regulatory information Management suite of products. + Knowledge of global regulatory requirements such as the FDA, EMA, and Health Canada. + An understanding of the drug development process for generics, branded and Non-Med product development? What do we offer you? + 25 days annual leave plus Bank Holidays + Company bonus scheme + Flexible benefits including health insurance, gymflex and cycle to work scheme + Programme of Wellbeing initiatives including on-site Creative Rooms, Employee Assistance Programme, Wellbeing Champions Function Regulatory Affairs Sub Function Medical Regulatory Affairs Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva's Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. EOE including disability/veteran

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