Job Details  
Advertiser: Leap 29


 
Job Title: Regulatory Associate - , UK
Location:Paddington
Rate:£0 Per Year
Description: Regulatory Associate - Paddington, UK

Location: UK
Start Date: End of August

Do you have a good level of Regulatory Affairs experience in the pharmaceutical industry?

Are you somebody who is able to motivate yourself working from home? Would this be the perfect opportunity as it offers flexible working hours? Read on to find out more about the role and experience required;

Role:

Reviewing registration data and dossiers for portfolio of new and mature products, populating spreadsheets, identifying gaps and work with client regulatory team to close gaps and complete registration datasets.
Two stages to the work:
1. Consolidate: This involves consolidating all the readily available date in a structured Excel. Client already have a master data spreadsheet and Kinapse will use this as a starting point.
2. Remediate: This involves using the consolidated data as a starting point to fill missing data, remove redundant data as well as confirm already captured data.
The data validation would be conducted by country per product and will involve collaboration with Client Regulatory Strategists and local RA.

Requirements
- 3 - 4 years of experiences in regulatory affairs working in the industry
- Attention to detail, data mining, data entry.
- Good working knowledge of CTD structure and location of data within a dossier.... Please go to https://www.aptrack.co/uap/AAAAbAAPV1gABZtU/ to see the full advert text.
Skills Required: Regulatory Associate - Paddington, UK
Job Type: Contract
Start Date: 08-08-2017
Contact: Prisca Olufunwa Contact E-mail: Click
Contact Tel: 000000000 Contact Fax:
Reference: J53043 Added: 08-08-2017
  IMPORTANT: For jobs based in the UK it is unlawful to employ a person who does not have permission to live and work in the UK. Please ensure you have this permission before applying, unless the advert states otherwise.
 
 
 
 
 
 
 
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