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

Planet Pharma; United Kingdom; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading global clinical research organization is seeking a Senior Medical Writer to create complex clinical documents crucial for regulatory submissions. This role involves collaboration with stakeholders, project management, and mentoring junior writers, offering a unique opportunity to contribute meaningfully to critical therapeutic developments.

Qualifications

• Experienced in authoring high complexity clinical documents like protocols and ICFs.
• Proven track record in medical writing, particularly as a project lead.
• Strong stakeholder and project management skills.

Responsibilities

• Author high complexity study-level documents including protocols and investigator brochures.
• Manage multiple projects while providing guidance to junior writers.
• Independently author clinical evaluation plans and reports for submissions.

Skills

Phase I - III protocol medical writing

Stakeholder management

Project management skills

Education

Experience as a medical writer

Job description

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

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

2 days ago Be among the first 25 applicants

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

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

As 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 be responsible for independently authoring:

• Clinical evaluation plans and Clinical evaluations reports
• Paediatric Investigational Plans (PIPs)
• Clinical summary 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 big part in bringing key therapies to market across a variety of therapeutic areas. You will be assigned to one sponsor and you will be leading on multiple projects, as well as supervising and providing guidance to more junior medical writers.

For this position, my client is looking for someone who has experience as a medical writer and has experience working as project lead on medical writing projects.

You will also have experience with:

• Phase I - III protocol and CSR medical writing experience
• Stakeholder management - both internal and external
• Project management/project lead skills

For more information on this position or any similar opportunities, please contact Chanel Hicken on 0203 868 1011 or email your updated CV to [e-mail] and we can arrange a time for a confidential discussion on how you can get involved in this exciting opportunity.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Writing/Editing, Science, and Research

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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