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Medical Writer/Editor (m/f)

Eingestellt von Hays aus Mannheim, Universitätsstadt

Gesuchte Skills: Design

Projektbeschreibung

REFERENZNUMMER:

295699/11

IHRE AUFGABEN:

-Edit other writers' work, check for scientific accuracy and grammatical or editorial errors
-Propose continuous improvements of the procedures and work instructions applicable within the department and when necessary, implement them
-Ensure in-depth review of clinical study documents for consistency (within and between documents), quality check, editing and formatting, in full compliance with relevant requirements: these documents will all be related to clinical studies (e.g. protocols, reports, investigator's brochures, ICFs, etc…)
-Contribute to the preparation of regulatory dossiers for submission to regulatory authorities, including writing, reviewing, formatting and editing the appropriate sections
-Ensure that scientific/clinical documents for external presentations (abstracts, posters) or for publication in peer-reviewed journals comply with the appropriate requirements (including reference styles and consistency)
-Ensure that clinical studies are registered on ClinicalTrials.gov and that the results of the terminated studies are disclosed
-Implement, maintain and improve the quality system: apply, review, update and create (if applicable) work instructions, standard operating procedures and document templates

IHRE QUALIFIKATIONEN:

-Advanced degree (or clinically relevant degree) in life sciences/healthcare
-Fluency in English (written)
-Excellent scientific/medical writing skills
-Excellent proficiency in Word, Reference Manager, Excel and Powerpoint softwares
-Capability to interpret, discuss and represent study- or program-related data
-Interpret and report results effectively
-Profound technical and operational experience in medical writing, preferably in the field of clinical research
-Strong interpersonal skills and good team player
-Ability to deliver in tight and changing timelines
-Good understanding of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process would be a plus

WEITERE QUALIFIKATIONEN:

Medical writer

Projektdetails

  • Einsatzort:

    Neuchâtel, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    24 MM

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

  • Kategorie:

    Medien/Design

  • Skills:

    design

Hays

  • Straße:

    Willy-Brandt-Platz 1-3

  • Ort:

    68161 Mannheim, Universitätsstadt, Deutschland