Cpl Life Sciences – Regulatory

Senior Associate, Report Publishing

7 days left

Location
Hatfield
Posted
22 Apr 2021
Closes
21 May 2021
Ref
JO-2104-466700
Contact
Charlie Harris
Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Senior Associate, Global Report Publishing
Location: Home-based with occasional travel to the office in Hatfield
Salary: Dependant on experience
Permanent position
Job Reference: JO-2104-466700

CPL Life Sciences are collaborating with a global pharmaceutical organization to hire a talented and career-driven report publisher. In this role, you will be responsible for the creation and maintenance of pharmaceutical product reports and be the primary support for the global submissions group. 

Responsibilities include;

  • Creation and maintenance of IMPDs, Protocols, Nonclinical and Clinical study reports.
  • Ensure all documentation is submissions ready
  • Collaborate with global colleagues to support to ensure quality submissions.
  • Maintain report publishing electronic archive


Requirements

  • 3+ years experience working within a regulatory publishing position
  • Knowledge of MS Office (Word, Excel, PowerPoint, Project), Adobe acrobat as well as being familiar with the use of regulatory system applications
  • Career driven & capable of working within a fast pace environment.
  • Good knowledge of electronic publishing systems



If you are interested in this role or would like more details please email your CV to Charlie.harris@CPL.com
Remember if this role is not suitable for you please feel free to forward this to anyone you feel would be suitable. If we successfully find a role for your recommendation we will give you £250 in vouchers of your choice.

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