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

Planet Pharma; United Kingdom; Remote; GBP 40,000 - 65,000; Full time

Job summary

A leading global clinical research organisation is seeking a Medical Writer II to author vital clinical documents. The role includes project management responsibilities and collaboration with stakeholders to ensure adherence to timelines, contributing to the success of key therapies in various therapeutic areas.

Qualifications

• Experience as a medical writer in Phase I - III protocols.
• Experience in project lead roles.
• Strong skills in stakeholder management.

Responsibilities

• Author study-level documents like protocols and investigator brochures.
• Interpret and summarise data for document preparation.
• Coordinate with stakeholders to ensure project timelines are met.

Skills

Medical writing

Stakeholder management

Project management

Job description

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

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

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Medical Writer II - 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 part of this role, you will be responsible for authoring most study-level documents including protocols, ICFs, lay summaries of clinical trial results, briefing packages, and investigator brochures. You will also be responsible for:

• Interpreting and summarising data
• Medical writing aspects of task finalisation including stakeholder alignment, coordination, and adherence to timelines.
• Representing medical writing in relevant project groups

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 get the chance to take project management responsibilities.

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

  Science, Research, and Writing/Editing

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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