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Job Details

PW-6778 Promotional Material Copy Review Lead

Company: AXESS
Reference: PW-6778
Closing Date: 29 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits: Bonus, Pension and Medical

Job Summary:

Opportunity for a pharmacist or medic to join this global Biopharmaceutical company in a role overseeing their Copy Review process. You’ll require previous copy review experience to lead and manage the Promotional Material process and perform related audits, act as key contact for the Zinc database and develop, mentor and run training sessions on the promotional material review process.?Permanent role, office based to the West of London.



Global Biopharmaceutical Company

Opportunity for a Medical / Copy Reviewer to move from Consultancy / Communications to Pharma

Opportunity to progress to final signatory for pharmacist or medic.



In this role you will

Lead and manage the Promotional Material process and perform related audits thereof

Act as key contact for the Zinc database

Develop, mentor and run training sessions on the promotional material review process

Undertake the review of promotional materials in the capacity of Regulatory Affairs reviewer in compliance with the ABPI code and EU regulation

Act as a backup and appropriate submission support to Regulatory Affairs Associates including?support regulatory submissions, approvals and reconciliation of Regulatory changes through to implementation. Status of dossier compliance to be assured at all times.



  • Fully conversant with Zinc software or similar application is strongly desirable. 
  • Ability to lead the Medical, Legal and Regulatory review process including training new starters, embedding the process across the business, identifying training needs, identifying process improvement and regularly auditing the process.
  • A Degree or Doctorate in health-related science, life science, Pharmacy.
  • Previous experience in promotional material review desirable and in Regulatory Affairs is preferred but it is not essential.?If you do not have experience in Regulatory Affairs you will have an interest to develop in this area and undertake regulatory tasks and act as a back-up for the Regulatory team.   
  • Excellent organisational, verbal, written and communication skills and the ability to work under pressure to tight deadlines.
  • Good knowledge of clinical data and clinical studies to be able to understand relevance of medical publication.
  • Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.



For a confidential discussion please telephone Jonathan Elliott at AXESS Limited on 020 8560 2300. To apply, please send your CV to quoting reference PW-6778.



Zinc/ Veeva/ Copy Reviewer / promotional reviewer / copy approver / pharma copy approver / regulatory affairs copy approver / regulatory submissions manager / copy approval manager / medical reviewer / medical review manager / medical review manager / copy approval associate / copy approval executive / M4 / M40 / London / Windsor / Slough / Maidenhead / Harrow / Hounslow / SW London / M4 Corridor



AXESS has been operating since 1990

We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development

We match professional candidates to the best permanent, contract and interim roles in the market

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Apply for this job:  PW-6778 Promotional Material Copy Review Lead

Contact Information:

Address:  Head Office
Isabella House,
12 Union Court,
Richmond upon Thames,
Tel:  +44 (0)20 8560 2300
Fax:  +44 (0)20 8560 2033
Website:  Visit Our Web Site

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