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Job Details

Regulatory Associate

Company: Clinical Professionals Ltd
Location: South East
Reference: J28776
Closing Date: 31 Aug 17
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

Regulatory Associate South England/Gloucestershire An exciting company who cover drug and device products and are going through a period of rapid growth and looking for a Regulatory Associate to join as soon as possible.

Requirements:

Regulatory Associate
Permanent
South England/Gloucestershire
£competitive


The Role
An exciting company who cover drug and device products and are going through a period of rapid growth and looking for a Regulatory Associate to join as soon as possible. The business is a global, publicly owned pharmaceutical company listed on AIM, part of the London Stock Exchange. They have been established for almost 20 years, and have grown to roughly £100 million annual turnover. The regulatory role is critical in supporting all aspects of Regulatory Affairs relating to the management of all products and thereby ensuring regulatory and commercial success. With excellent benefits and opportunities for progression and learning, the organisation are keen to consider more junior applicants looking to get their first foot in the door. This is a very unique opportunity for someone looking to develop their career in the field of regulatory affairs.

Key Accountabilities:
- Responsible for, a complete and accurate database which includes data entry and/or QC, report and metrics (such as Regulatory Database). This may also include administrator rights.
- Support the preparation, submission and tracking of documents and analyse / transform data into the relevant format (such as preparation of article 61(3) applications, variations, renewals, PSURs).
- Support product information repositories.
- Support and may be responsible for the management of some systems and processes.
- Support and may be responsible for, the maintenance and QC of product information.
- Support and may be responsible for, projects (such as due diligence and integration of acquisition projects).
- Support and may be responsible for, the QMS.
- Input into ongoing training and professional development activities in order to fulfil departmental goals and objectives. Responsible for, the training of others which may include mentoring.
- Understanding of, and may optimise relationships with, internal customers.
- Act to identify issues / propose solutions/ may implement.
- Input into time management and work prioritisation.
- Provides technical knowledge.
- Understanding of external environment.
- Act to ensure, and may optimise, business and its needs.
- Understand best practise and make recommendations.

Essential Requirements:
* Life science or pharmacy degree
* Some exposure to or knowledge of regulatory affairs preferred
* Eligibility to work in the UK
* Full UK driving licence
* Fluent in English and excellent communication skills both written and verbal



Please visit www.clinicalprofessionals.co.uk/search for more vacancies or general market information.

If you are not actively looking, we have contacted you because we value your experience and thus your opinion regarding recommendations. We offer a generous reward for any candidate you refer who goes on to be successfully placed in one of our positions. This is a great chance for you to assist somebody in fulfilling their potential for 2017!

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Apply for this job: Regulatory Associate

Contact Information:

Address:  Clinical Professionals UK
3rd Floor
33 Blagrave Street
Reading
Berkshire
RG1 1PW
England
Tel:  0044 118 959 4990
Fax:  0044 118 956 0607
Website:  Visit Our Web Site

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