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- Tasks: Create and manage clinical documents like protocols and summaries for trials.
- Company: Join a leading global clinical research organisation making a difference in healthcare.
- Benefits: Enjoy remote work flexibility and the chance to lead exciting projects.
- Why this job: Be part of a team that brings innovative therapies to market and impacts lives.
- Qualifications: Experience in medical writing and project management is essential.
- Other info: Work closely with stakeholders and take ownership of your projects.
The predicted salary is between 28800 - 48000 £ per year.
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 chanel.hicken@planet-pharma.co.uk and we can arrange a time for a confidential discussion on how you can get involved in this exciting opportunity.
Medical Writer II - Global Clinical Research Organisation - Home based in UK employer: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Writer II - Global Clinical Research Organisation - Home based in UK
✨Tip Number 1
Familiarise yourself with the specific types of documents you'll be writing, such as protocols and investigator brochures. Understanding the nuances of these documents will help you demonstrate your expertise during interviews.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who work as medical writers. Engaging with them on platforms like LinkedIn can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Brush up on your project management skills, as this role requires leading medical writing projects. Consider taking a short course or obtaining a certification that highlights your ability to manage timelines and stakeholder expectations.
✨Tip Number 4
Prepare to discuss your experience with stakeholder management in detail. Be ready to share examples of how you've successfully collaborated with both internal teams and external clients to achieve project goals.
We think you need these skills to ace Medical Writer II - Global Clinical Research Organisation - Home based in UK
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Medical Writer II. Familiarise yourself with the types of documents you'll be expected to author, such as protocols and investigator brochures.
Tailor Your CV: Highlight your relevant experience in medical writing, especially any project management roles you've held. Make sure to include specific examples of your work on Phase I - III protocols and CSR documents.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention your experience with stakeholder management and how it aligns with the job requirements. Be sure to convey your passion for contributing to clinical research.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter. Ensure there are no grammatical errors or typos, as attention to detail is crucial in medical writing. A polished application reflects your professionalism.
How to prepare for a job interview at LinkedIn
✨Showcase Your Medical Writing Experience
Be prepared to discuss your previous medical writing projects in detail. Highlight specific documents you've authored, such as protocols and investigator brochures, and explain your role in the project management process.
✨Demonstrate Stakeholder Management Skills
Since stakeholder alignment is crucial for this role, come equipped with examples of how you've successfully managed both internal and external stakeholders in past projects. This will show your ability to coordinate effectively.
✨Familiarise Yourself with Clinical Trial Phases
Brush up on your knowledge of Phase I-III clinical trials and the associated documentation. Being able to discuss these phases confidently will demonstrate your expertise and understanding of the medical writing landscape.
✨Prepare Questions About Project Management
As project management is a key aspect of this role, prepare insightful questions about the project management processes used by the organisation. This shows your interest in the role and your proactive approach to understanding their workflow.
