IT Regulatory Affairs Project Manager - Slough - 6 Months Initially - £585 per day
Recruiter
ABWRecruitment
Listed on
11th May 2021
Location
Slough
Salary/Rate
Upto £585
Type
Contract
This job has now expired please search on the home page to find live IT Jobs.
My Client a Leading Pharmaceutical comapny based in Slough requires an IT Regulatory Affairs Project Manager Who we are: The IT Development solution team defines the IT-RA (Regulatory Affairs) roadmap and manages the IT-applications and projects for the Regulatory Affairs team. The team is also the IT point-of-contact for the Regulatory Affairs team for all IT questions and requests.The candidate will carry on an already started large waterfall and GxP project, organized in interconnected streams along 4 dimensions: Data, people, processes & tool. The direct stakeholders are from my clients Regulatory Affairs, My clients IT functional & technical teams on-site and remote and with the supplier (Veeva). The main tasks will be: Drive and manage the successful implementation, migration & validation activities of a Veeva Registrations project with the Regulatory Affairs department. Manage, with the RA project manager & stakeholders, the delivery of the remaining configuration, data migration, interfaces, reports and the related documentation. The candidate is requested to go into the content of the project to grasp the impact, the dependencies, priorities, scope, etc. Follow-up of the different (external) technical team(s) and the supplier during implementation and be on top of the situation Coordinate with the validation lead with design, review, and approval of test plans and test scripts Follow-up (cost, time, scope, risks, dependencies, priorities, etc.) of the project Prepare the key messages for the steering committee, drive the project management team meetings Communicate relevant information & statuses every fortnight to the stakeholders Coordinate the activities and deliveries, propose solutions where necessary, share meeting notes, make the projects happen. Required experience of at least 3 years: Proven project management experience Proven experience with IT- projects in a GxP environment Proven experience with RA-processes and terminology in a (bio)-pharma environment Knowledge of Veeva RIM Registrations is a plus Ability to connect & communicate with technical and non-technical experts Driven by the motivation to deliver results Ambition to work independently and to structure workload Proven IT experience: MS Office, project management tools Fluent in English
Due to Covid-19, home working is now advised until further notice.
This is a full-time role.
Starting date: the latest 25th May Initial contract: Beginning May 2021 to end Dec 2021
