Regulatory Knowledge Specialist
- Employer
- CK Group
- Location
- Slough
- Salary
- £45-55 per hour
- Closing date
- 6 Oct 2020
View more
- Sector
- Regulatory Affairs
- Contract Type
- Contract
- Hours
- Full Time
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Job Details
CK Clinical are recruiting for a contract Regulatory Knowledge Specialist to join a pharmaceutical company at their site based in Slough on a contract basis for 12 months.
The Company:
Our client is a multinational patient-focused biopharmaceutical company that focus on severe diseases.
The Location:
The role is based at our client's site in Slough, which is easily commutable from London and the surrounding areas.
Regulatory Knowledge Specialist Role:
The main purpose of the role will be to:
- Strategize and execute data enhancement initiatives, contributing to design elements for data process and system behaviours.
- Support and coordinate global registration information in various software management tools (Liquent Insight Manager and FirstDoc).
- Execute regulatory tracking tasks and events in the database (submissions, response to questions, approvals, and withdrawals).
Your Background:
To succeed in this role:
- You will come from a Regulatory Affairs background in processing of Regulatory Information Management (RIM).
- Experience is required in supporting end users to enter and maintain product information in a registration tracking database.
Apply:
For more information or to apply for this Regulatory Knowledge Specialist position, please contact CK Group, quoting job ref 48324.
It is essential that applicants hold entitlement to work in the UK.
The Company:
Our client is a multinational patient-focused biopharmaceutical company that focus on severe diseases.
The Location:
The role is based at our client's site in Slough, which is easily commutable from London and the surrounding areas.
Regulatory Knowledge Specialist Role:
The main purpose of the role will be to:
- Strategize and execute data enhancement initiatives, contributing to design elements for data process and system behaviours.
- Support and coordinate global registration information in various software management tools (Liquent Insight Manager and FirstDoc).
- Execute regulatory tracking tasks and events in the database (submissions, response to questions, approvals, and withdrawals).
Your Background:
To succeed in this role:
- You will come from a Regulatory Affairs background in processing of Regulatory Information Management (RIM).
- Experience is required in supporting end users to enter and maintain product information in a registration tracking database.
Apply:
For more information or to apply for this Regulatory Knowledge Specialist position, please contact CK Group, quoting job ref 48324.
It is essential that applicants hold entitlement to work in the UK.
Company
Find the career you always dreamed of
We are the CK Group, the UK’s specialist in scientific, clinical and technical recruitment.
We have 4 brands:
- CK Science is the leading independent scientific recruitment consultancy.
- CK Clinical is an established leader in the clinical research and drug development sectors
- CK Technical specialises in jobs for Engineers and IT professionals
- CK QLS finds roles for high calibre professionals working in the science and technology sectors in Switzerland.
Over the last 28 years we have found jobs for thousands of high calibre scientists in the scientific, chemical, waste, biotechnology and pharmaceutical industries. By working with us to find your next job, you will get access to the best scientific vacancies in the UK, Europe and the rest of the world.
We are proud to be working with 18 out of the world’s top 20 scientific organisations.
We can help you find your dream job.
ckscience.co.uk
Company info
- Website
- http://www.ckscience.co.uk/
- Telephone
- +44 (0)1246 457700
- Location
-
CK Group
Westwick House
The Bridge Business Centre
Beresford Way
Chesterfield
S41 9FG
GB
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