Medical Writer
Geneva, CH
vor 3 Tg.

My client is an innovating, dynamic and growing international medical device company currently expanding their clinical team in Switzerland, Geneve Canton.

Due to this growth my client is looking for a Medical / Scientific Writer.

The position will report to the Head of Clinical Development Department.

Your Responsabilities :

Prepares and finalises clinical documents such as, but not limited to, CSRs and appendices, IBs, protocols and protocol amendments, summary documents, RMPs (initial and updates), regulatory responses, and briefing documents.

  • Documents must be of high quality in terms of scientific content, as well as organisation per regulatory and internal guidance, clarity, and accuracy, with attention to format and consistency;
  • Leads cross-functional document planning and review meetings

  • Leads in a team environment with greater independence for longer-term activities, and takes a lead role on assigned projects concerning timing, scheduling, and tracking;
  • Indirectly or directly leads or sets objectives for others on team projects and tasks; e.g., able to lead process working groups;
  • The primary point of contact for Clinical Development Team for medical writing activities;
  • Responsible for functional planning and metrics database updates for assigned program.

    Ihr Profil :

    PhD or Master in elated Pharmaceutical Science with minimum 3 years experience of relevant regulatory medical writing

  • Ability to function (and potentially lead) in a team environment;
  • Demonstrates learning agility ;
  • Builds solid and productive relationships with cross-functional team members;
  • Strong project management skills

    Strong leadership skills

    Fluent in English and French

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