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

JR United Kingdom; Belfast; Remote; GBP 40,000 - 60,000; Full time

Job summary

Join a globally renowned clinical research organization as a Medical Writer II, working from home in Belfast. In this role, you'll author critical clinical documents and manage projects while collaborating with stakeholders. Ideal candidates will have medical writing experience and project leadership skills.

Qualifications

• Experience as a medical writer and project lead on medical writing projects.
• Familiarity with Phase I-III protocol and CSR medical writing.

Responsibilities

• Author study-level documents including protocols, ICFs, and investigator brochures.
• Interpret and summarize data, ensuring stakeholder alignment.
• Represent medical writing in relevant project groups.

Skills

Medical writing

Stakeholder management

Project management skills

Job description

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

Planet Pharma is currently working with a global clinical research organisation (CRO) that is looking for an experienced Medical Writer to join the team and support 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 significant role in bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor and have the chance to take on project management responsibilities.

For this position, the client is seeking someone with experience as a medical writer and as a 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/project lead skills

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