Job Ref: 214046300

Date: 2021-06-23 16:49:07

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My Client, a global Pharmaceutical business has a great opportunity for a Regulatory Information Analyst to join the Lifecycle registration team on a six month contract at their High Wycombe facility.

As Regulatory Information Analyst, you will:

Providing support for the Product and Lifecycle Registration (PLcR) for Registrations software platform
Global duties focused on supporting the data needs in EU, US and Rest of the World
Join a small team of regulatory data specialists, working independently in a virtual and matrixed environment
Retrieving data using queries and reports, as well as resolving complex data issues

To be considered for the role of Regulatory Information manager, you will:

Educated to Degree level in Life Sciences of Data Management
2 years experience in relevant regulatory process
XEVMPD submissions essential
Knowledge of Article 57
Detail oriented, sharp and focused communication skills
Experience of working with InSight for Registrations highly desirable

The role is based at High Wycombe in the UK on an Initial contract for 6 months with possibility for a 6-months extension based on business needs.

Applicants must hold valid right to work status and be commutable to site.

INSIDE IR35 ONLY.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business

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