Regulatory Medical Writer

hace 1 semana


Madrid, Madrid, España Thornshaw Scientific Recruitment A tiempo completo
Posted date 03 May 202- LocationMadrid

  • Job type Permanent
  • SalaryNegotiable
  • Discipline Life Sciences
  • ReferenceJO

Regulatory Medical Writer

Location - Anywhere in Europe (Fully Remote)
An exciting opportunity to join an established CRO and work at the fourth front of innovation.

As a Regulatory Medical Writer, you will be working within a collaborative and interactive medical writing team and will work with colleagues all across Europe.


This is an excellent opportunity for a junior/ trainee Medical Writer to step into a more senior position and take the lead on writing activities.

The business has some very exciting projects working with leading Pharma/ Biotech clients working on oncology and rare disease projects.


Responsibilities

  • Writing, authoring, and owning Clinical and Regulatory documents (Clinical Study Reports, Protocols, and other regulatory documentation.)
  • Work in a collaborative team with multiple different projects happening at once.
  • Support colleagues but also be able to work alone.

Experience

  • 2 to 3 years of relevant medical writing experience.
  • Experience writing CSR and Protocols.
  • Strong internal clientfacing experience, a good consultative approach, and strong communication skills are a must.
  • Must be able to demonstrate working on multiple streams of work.
  • A French speaker would be desirable.


A very exciting opportunity to work for an established CRO and work within a team that will support you with guidance and development plans.

The role also comes with an excellent benefits scheme and the flexibility of working fully remotely.
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