Senior Medical Writer - Global Clinical Research Organisation - Home based in UK

JR United Kingdom; Nottingham; Remote; GBP 55,000 - 80,000; Full time

Job summary

Une organisation de recherche clinique mondiale recherche un Senior Medical Writer pour rédiger des documents d'essai cliniques complexes et superviser des projets. Vous jouerez un rôle clé dans l'introduction de nouvelles thérapies sur le marché, tout en travaillant en étroite collaboration avec des parties prenantes internes et externes.

Qualifications

• Expérience en rédaction médicale et en tant que leader de projets.
• Connaissances dans les protocoles de phases I à III et écriture de CSR.
• Compétences en gestion des parties prenantes, internes et externes.

Responsibilities

• Rédaction de documents cliniques complexes tels que programmes et résumés.
• Supervision et formation des rédacteurs médicaux juniors.
• Gestion de multiples projets avec un sponsor.

Skills

Rédaction médicale

Gestion de projet

Gestion des parties prenantes

Job description

Social network you want to login/join with:

Senior Medical Writer - Global Clinical Research Organisation - Home based in UK, Nottingham

Planet Pharma is currently working with a global clinical research organisation (CRO) that is looking for an experienced Medical Writer to join their team and support the preparation of submission and other complex clinical documents.

As a Senior Medical Writer, you will be responsible for authoring high-complexity study-level documents including protocols, ICFs, investigator brochures, and meeting packages. You will also independently author:

• Clinical evaluation plans and reports
• Paediatric Investigational Plans (PIPs)
• Clinical summaries and overview documents in CTD/eCTD formats for global regulatory submissions

This is an exciting opportunity to join a globally renowned CRO and play a significant role in bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor, leading multiple projects, and supervising and guiding junior medical writers.

For this position, the client is looking for someone with experience as a medical writer and project lead on medical writing projects.

You should also have experience with:

• Phase I - III protocol and CSR medical writing
• Stakeholder management - internal and external
• Project management and leadership skills

For more information or to apply, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We can arrange a confidential discussion on how you can get involved in this exciting opportunity.