Posted to MedZilla on 4/28/2017


England, Senior Regulatory Associate RA_PD_11662-MZ


This vacancy is for a Senior Regulatory Associate job at a leading multinational biopharmaceutical company with leading therapies in autoimmune diseases and oncology. This role will be based at their offices in Uxbridge, UK and is an exciting opportunity to work for one of the world's biggest biotechnology firms that is regularly included on numerous best employers' lists worldwide.  

Job Role:

The Regulatory Professional under the direction of a Regional Regulatory Lead will assist in the creation and submission of regulatory documents and may be the regulatory lead for a program under the supervision of a more experienced regulatory lead.

Role Responsibilities:

  • Assist Regional Regulatory Lead to support regional regulatory pre-filing activities (e.g. core CTA/IMPD development and submission, support for pre-MAA filing, regulatory authority meeting preparations)
  • Provide and maintain CTA/MA documentation support (e.g. variations, substantial amendments, PDCO annual reports) in collaboration with Regional Regulatory Lead Create and maintain product regulatory history documents through IMR/rRISE and appropriately archive all regulatory documents and agency communications
  • Review regional component of the Global Regulatory Plan and provide input to operational deliverables
  • Ensure compliance via timely submissions to regulatory agencies Support RRL in review of promotional materials for commercial activities (ex-US) Collaborate with CROs / partners to support site initiation Coordinate collection of functional documents in support of regulatory applications
  • As appropriate participate in GRT to support execution of regulatory strategy
  • Coordinate QC of regulatory documentation (e.g. briefing packages)
  • Provide primary authorship to routine regulatory correspondence (e.g. annual reports, investigator packages)
  • Prepare regulatory packages and cross-reference letters to support investigator initiated studies
  • Approve drug shipment for company and Investigator Initiated Studies
  • Complete regulatory forms to support agency communications (E.G. EudraCT,)
  • Provide regulatory support to Commercial, Medical and Clinical departments through cross-functional interactions in brand and therapeutic area teams
  • Support process improvement initiatives, standards development, and metrics
  • Assist in template development and maintenance
  • Respond to specific requests from and communicate relevant issues to GRT Develop Regulatory Position with teams
  • Actively support regulatory compliance Support the development and execution of GRT goals

Education, Skills and Experience:

  • Bachelor's degree and 3 years of directly related experience
  • Experience supporting regional regulatory leads, including direct interaction with regulatory agencies
  • Strong communication skills
  • Oral and written
  • Understanding of drug development process
  • Regulatory principles
  • Working with policies, procedures and SOP's
  • Knowledge of legislation and regulations relating to medicinal products
  • Awareness of the registration procedures in region for MA, post approval changes, extensions and renewals.
  • Knowledge of drug development
  • Cultural awareness and sensitivity to achieve results across both regional country and International borders.

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 call Peter Duvall on +44 203 0789 542 or upload your CV on our website
A full job description is available on request.
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