Medical Writer

Project-ID: 1326

Your activities

  • Writing clinical documents for submission to regulatory authorities
  • Promote the document drafting process
  • Receive and review primary statistical material, draft documents for review, and include/clarify comments with all reviewers
  • Conduct literature searches to support writing activities
  • Supporting project teams by providing scientific/medical advice
  • Medical and editorial review of drafts and final documents prior to distribution
  • Coordinate and work closely with Medical Experts within the organisation
  • Oversee documents that have been outsourced to other medical writing CROs

Your background

  • Completed scientific studies
  • Solid experience in the field of medical writing (oncology indication would be a plus)
  • Strong knowledge of writing guidelines (e.g. EMA, FDA, ICH, AMA, etc.)
  • Solid experience with global marketing authorisation applications for medicinal products
  • Excellence written and spoken English skills
Gender note

For reasons of better readability the language forms masculine, feminine and diverse (m/f/*) are used simultaneously. All references to persons apply equally to all genders.

Type of contract

Permanent

Industry

Pharmaceuticals

Department

Medical Affairs

Location

Remote

Germany

Entry date

ASAP

Duration

Permanent

Remote

ja

Capacity (FTE)

1

Your contact person
KGU_neu
Karoline Gutensohn

Senior Recruitment Managerin

Interested?

We are looking forward to your application!

To apply, simply fill out the contact form below and attach your resume.

Your CV