Senior Associate- Regulatory Affairs

£25 - £35 per hour
  1. Permanent
  2. Officer /Associate
  3. United Kingdom
Cambridge, England
Posting date: 09 Sep 2019
RA.NS.25201_1568030095

A vacancy has arisen for a Senior Associate - Regulatory Affairs job at a leading multinational biopharmaceutical company with leading therapies in autoimmune diseases and oncology. They are seeking an individual to bring solid regulatory affairs experience their team at their offices in Cambridge. This is an exciting opportunity to work for one of the world's biggest biotechnology firms that employs over 17,000 staff globally.

Job Responsibilities:

  • 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.
  • 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 Amgen 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.

Skills and Requirements:

  • Understanding of drug development process.
  • 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 Numhom Sudsok at +44 203 871 8093 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

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

Proclinical Staffing is an equal opportunity employer.

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