Regulatory Documentation Scientist

Negotiable
  1. Interim/Contract
Welwyn Garden City, England
  1. PVG & Drug Safety, Drug Safety Writing
Posted: 13/12/2022
BBBH20983

This vacancy has now expired. Please see similar roles below...

Hobson Prior are currently looking for a Regulatory Documentation Scientist to join a brilliant pharmaceutical establishment on a contract basis. Our client is focused on providing life-changing remedies for various illnesses.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

  • For this role, you will handle the planning of a suite of regulatory papers such as clinical dossiers, suite of safety reports, etc.
  • Serve as a mentor to new personnel in the documentation team.
  • Guide the writing/editing team on planning clinical reports/safety dossiers.
  • You will plan specifications for outsourced such as writing/evaluating documents, as well as serve as the company's liaison for project reasons.
  • Partake in best practice and consistent improvement in regulatory documentation.
  • The deal candidate will serve as a representative for the group within functional and cross functional initiatives/projects where needed.
  • Prepare and produce timelines for the generation of allocated papers such as clinical reports/suite of safety papers, etc.
  • Guarantee proper planning and resourcing of all papers allocated to the writing/editing team which involves work to be outsourced.
  • Any other assigned duties.

Key Skills:

  • Project management abilities.
  • Ability to work on various tasks simultaneously and deliver tasks on deadlines.
  • Interpersonal and communication skills both verbally and in writing.
  • Capable of influencing without authority.
  • Works well in a team setting with the ability to resolve issues.
  • Able of leading the work of others.

Requirements:

  • Educated to a degree level in a life science or similar discipline.
  • Able to exhibit a clear, high-quality, scientific writing style in English.
  • Familiarity with regulatory affairs or connected functions in drug development.
  • Know-how of global guidelines.
  • Prior involvement in writing and/or editing regulatory papers.
  • Able to analyse as well as synthesise data from a variety of fields independently.
  • Willing to travel for business needs.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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