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- Tasks: Lead the creation of clinical documents and manage writing projects in a dynamic environment.
- Company: Join a leading global organisation in the life sciences sector, making a real impact.
- Benefits: Enjoy a collaborative culture with opportunities for professional growth and development.
- Why this job: Be at the forefront of clinical research, shaping the future of healthcare.
- Qualifications: 3+ years in medical writing, including project leadership experience in pharma or CRO.
- Other info: Contact Ollie at Planet Pharma for more details or to apply.
The predicted salary is between 36000 - 60000 £ per year.
Our client, a leading global organization in the life sciences sector, is seeking an experienced Medical Writing Project Lead to support the development of clinical documentation across various study phases, with a focus on Phases I–III protocols and clinical study reports (CSRs). This role offers the opportunity to lead study-level writing tasks and collaborate cross-functionally in a dynamic, highly regulated environment.
Key Responsibilities:
- Independently create a range of clinical documents, including study protocols, informed consent forms (ICFs), clinical study reports (CSRs), layperson summaries, briefing materials, and Investigator Brochures.
- Assist senior medical writers with the preparation of complex or high-level submission documents.
- Analyze and interpret clinical data to produce clear, accurate, and scientifically sound content.
- Lead discussions around document development, ensuring strategic alignment and effective stakeholder input.
- Coordinate and facilitate meetings to drive decisions and advance medical writing deliverables.
- Uphold high standards of quality, accuracy, and compliance with both regulatory guidelines and internal procedures.
- Act as a representative for the medical writing function in cross-functional project meetings.
- Oversee timelines, manage stakeholder feedback, and guide documents through review and finalization.
- Adhere to internal SOPs and client-specific processes throughout the document development lifecycle.
- Support process enhancements and contribute to collaborative knowledge sharing across teams.
Required Skills & Experience:
- A minimum of 3 years’ medical writing experience within the pharmaceutical or CRO sector, including at least 1 year in a project leadership role.
- Solid understanding of clinical research processes, regulatory requirements, and documentation standards.
- Proven track record of independently managing medical writing projects from start to finish.
- Strong interpersonal and communication skills, with the ability to effectively engage stakeholders at all levels.
- Self-motivated and resourceful, with a proactive and problem-solving approach to challenges.
- Capable of guiding content discussions, aligning teams, and facilitating decisions.
- Highly organized, with excellent time management and the ability to juggle multiple projects simultaneously.
- Comfortable interpreting complex data sets and presenting them in clear, regulatory-compliant formats.
- Experienced in navigating SOPs, templates, and regulatory frameworks in a structured work environment.
This is an excellent opportunity for a motivated medical writer to lead impactful projects and contribute to global clinical programs.
Medical Writer employer: JR United Kingdom
Contact Detail:
JR United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Writer
✨Tip Number 1
Network with professionals in the pharmaceutical and clinical research sectors. Attend industry conferences, webinars, or local meetups to connect with potential colleagues and learn about job openings that may not be advertised.
✨Tip Number 2
Join relevant online forums and social media groups focused on medical writing and clinical research. Engaging in discussions can help you stay updated on industry trends and may lead to job referrals.
✨Tip Number 3
Consider reaching out directly to hiring managers or team leads at companies you're interested in. A well-crafted message expressing your interest in their work can set you apart and potentially open doors for opportunities.
✨Tip Number 4
Stay informed about the latest regulatory guidelines and documentation standards in medical writing. Demonstrating your knowledge during interviews can showcase your commitment to quality and compliance, making you a more attractive candidate.
We think you need these skills to ace Medical Writer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your medical writing experience, especially the three years required in the pharmaceutical or clinical research sector. Emphasise any project leadership roles you've held and specific documents you've created.
Craft a Compelling Cover Letter: In your cover letter, explain why you're passionate about medical writing and how your skills align with the job requirements. Mention your experience with clinical documentation and your ability to lead discussions and coordinate projects.
Showcase Relevant Skills: Clearly outline your understanding of clinical research processes and regulatory requirements. Provide examples of how you've managed medical writing projects from start to finish, and highlight your strong communication skills.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Ensure there are no grammatical errors or typos, as attention to detail is crucial in medical writing. A polished application reflects your commitment to quality.
How to prepare for a job interview at JR United Kingdom
✨Showcase Your Experience
Make sure to highlight your 3+ years of medical writing experience, especially your project leadership role. Be prepared to discuss specific projects you've led and the impact they had on clinical documentation.
✨Understand Regulatory Requirements
Familiarise yourself with the regulatory guidelines relevant to clinical research. During the interview, demonstrate your knowledge of these standards and how you ensure compliance in your writing.
✨Prepare for Data Interpretation Questions
Since the role involves analysing clinical data, be ready to discuss how you interpret complex data sets. You might be asked to explain how you would present this information clearly and accurately in your documents.
✨Emphasise Communication Skills
Strong interpersonal skills are crucial for this role. Prepare examples of how you've effectively engaged stakeholders and facilitated discussions in previous projects, showcasing your ability to align teams and drive decisions.
