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

JR United Kingdom; Slough; Remote; GBP 40,000 - 65,000; Full time

Job summary

A leading global clinical research organization is looking for an experienced Medical Writer II to prepare essential clinical documents as part of their team. This role offers the chance to take on project management responsibilities, working closely with stakeholders to bring therapies to market across various therapeutic areas.

Qualifications

• Experience as a Medical Writer II with Phase I - III protocol and CSR writing experience.
• Background in project management and leading medical writing projects.
• Strong stakeholder management skills.

Responsibilities

• Author study-level documents including protocols and investigator brochures.
• Interpret and summarize data while ensuring adherence to timelines.
• Represent medical writing in relevant project groups.

Skills

Medical writing

Interpersonal skills

Project management

Stakeholder management

Education

Relevant degree in life sciences

Job description

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

Client:

Planet Pharma

Location:

slough, United Kingdom

Job Category:

Other

Online job hunting tools

-

EU work permit required:

Yes

Job Views:

2

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

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.

Online job hunting tools

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.

Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit. Check our Blog for more information.

Bank or payment details should not be provided when applying for a job. Eurojobs.com is not responsible for any external website content. All applications should be made via the 'Apply now' button.

Created on 04/06/2025 by JR United Kingdom