EMEA Medical Compliance Advisor

Highly Competitive
  1. Permanent
  2. Medical Advisor
  3. United Kingdom
Hatfield, Hertfordshire
Posting date: 17 Jul 2019
ME.DM.24366_1563366347

A leading pharmaceutical client is searching for an EMEA Medical Compliance Advisor to join their team in the UK. The company specialises in various therapy areas including oncology, neurology and gastroenterology, and employs several thousand across the globe.

Job Responsibilities:

  • Support implementation of medical compliance programme for UK / ROI and EMEA Business Groups.
  • Develop or rewrite SOPs related to Code compliance and ensure all relevant staff receive adequate training.
  • Manage CAPA register, identify areas of risk and in consultation with EMEA Medical Compliance Manager implement risk mitigation plans.
  • Ensure systems and processes are in place to control and monitor compliance with ABPI /IPHA Codes and company policies.
  • Proactively champion and lead awareness of the Codes of Practice and related processes and policies throughout the company to ensure high level of competence and understanding.
  • Support EMEA Medical Compliance Manager in driving strong compliance culture.
  • Report compliance breaches to and liaise with the EMEA Corporate Compliance Department.
  • Maintain up-to-date knowledge of relevant Codes of Practice and legislation including (but not limited to) ABPI / IPHA / EFPIA Codes of Practice, MHRA Blue Guide and Company SOPs to ensure adherence in all areas as appropriate.
  • In consultation with EMEA Medical Compliance Manager oversee electronic copy approval system to ensure any appropriate developments within the system are implemented.
  • Manage assigned projects.
  • Advise and train (or support training) of non-EKC based colleagues on interactions with UK/ROI based HCPs.

Skills and Requirements:

  • Experience working in pharmaceutical industry, ideally in compliance role.
  • Familiarity with components of compliance programme
  • Knowledge of the ABPI, IPHA and EFPIA Codes of Practice and compliance requirements
  • Experience in writing and reviewing SOPs.
  • Experience in managing deviations and CAPAs.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Divya Mistry at +44 20 3814 1315 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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