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Job Details

Regulatory Data Analyst - London

Company: CK Clinical
Location: London
Reference: CL40450
Closing Date: 24 Nov 17
Type: Contract
Salary (£): Competitive
Benefits:

Job Summary:

Mary Bolt is recruiting for a Regulatory Data Analyst to join a leading, patient focused, global pharmaceutical company at their site based in London on...

Requirements:

Mary Bolt is recruiting for a Regulatory Data Analyst to join a leading, patient focused, global pharmaceutical company at their site based in London on a 6 month contract basis.

The main purpose of the role will be to:
-Develop a good understanding of the RIM system and reports from the system to be able to update the data and develop a good understanding of other GRA systems to the level needed to perform the role.
-Work with RIM (Snr) Information Analysts to ensure data supplied to RIM is in accordance with data standards & governance.
-Work thoroughly and consistently through the allocated work load to ensure complete and accurate entry/ loading of data/ documents into GRA systems.

Further responsibilities will include:
-Ensuring that data is entered into the company's GRA system(s) in accordance with processes and data quality standards as documented in the relevant Job Aids / WIs / Data Governance Plan.
-Consulting within SIM and with information suppliers to resolve adhoc quality issues and queries on the data/ documents provided.
-Applying business rules consistently and in line with relevant Job Aids / WIs and raising all exceptions to RIM (Snr) Information Analysts for resolution.

In order to be considered for this role, you will be required to have the following qualifications, skills and experience:
-Ideally educated to degree level or above in life science, sciences or a related field.
-Experience of operating in a Pharmaceutical, Regulatory Affairs organization and working in a GxP related pharmaceutical environment as well as experience of extracting and manipulating data from SQL or similar database management systems and experience of the drug development and regulatory dossier creation, review and approval process.
-A thorough understanding of general IT tools (Microsoft Office, Window's Explorer, file management, etc), an excellent understanding of Microsoft Excel including use of advanced features including, functions, pivot tables and macros and athorough understanding of database principles (e.g. Entity relationships, referential integrity).

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL40450 in all correspondence.

Apply for this job: Regulatory Data Analyst - London

Contact Information:

Address:  Head Office
9 High Street
Stevenage
Hertfordshire
SG1 3BG
England
Tel:  +44 (0)1438 743047
Fax:  +44 (0) 1438723800
Website:  Visit Our Web Site

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