Clinical Protocol/ Medical Writer (Yacht Life Sciences)

Clinical Protocol/ Medical Writer (Yacht Life Sciences)

Yacht

Onbekend
bijna 5 jaar geleden
Elektromonteur duurzame energietechniek

Elektromonteur duurzame energietechniek

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Audiovisueel monteur

Audiovisueel monteur

Eminent

Permanent
ongeveer 1 maand geleden
Paneelbouwer

Paneelbouwer

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Permanent
ongeveer 1 maand geleden
Project engineer automatisering

Project engineer automatisering

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Elektromonteur e&i

Elektromonteur e&i

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Leidinggevend elektromonteur / voorman

Leidinggevend elektromonteur / voorman

Eminent

Permanent
ongeveer 1 maand geleden
Service technicus e&i

Service technicus e&i

Eminent

Permanent
ongeveer 1 maand geleden
Software (automation) engineer e&i

Software (automation) engineer e&i

Eminent

Permanent
ongeveer 1 maand geleden
Leidinggevend elektromonteur e&i

Leidinggevend elektromonteur e&i

Eminent

Permanent
ongeveer 1 maand geleden
Elektromonteur e&i

Elektromonteur e&i

Eminent

Permanent
ongeveer 1 maand geleden
Clinical Protocol/ Medical Writer (Yacht Life Sciences)

Clinical Protocol/ Medical Writer (Yacht Life Sciences)

Yacht Soest (3768MN)

Contract: Uren: 40 - 40Salaris:

Job description

Yacht Life Sciences has a vacancy for an experienced Medical Writer. For the Medical Writing team of our client, we are looking for a (freelance/ ZZP) Medical Writer who will focus on writing clinical protocols and protocol amendments. This is a fully home-based position.


The responsibilities of the Protocol Writer may include, but are not limited to the following:

  • Works independently to write and edit clinical protocols and protocol amendments.
  • Negotiates timeline development for preparation of clinical protocols and amendments.
  • Leads the process of critical review of clinical protocols and incorporates multiple reviews into successive drafts.
  • Provides QC support for clinical protocols as needed.
  • Assists with or leads the preparation or revision of SOPs, WPDs, and document templates. Assists with training across functional areas for the implementation of new/revised procedures and templates.
  • Participates in clinical project team meetings.
  • Participates in or leads other cross-functional team meetings and standards committees.
  • Ensures the quality of clinical protocols by maintaining and promoting familiarity with ICH, GCP, and other standards.
  • Writing and editing clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical regulatory documents across multiple therapeutic areas could be assigned as well.