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- Tasks: Lead medical writing projects, ensuring high-quality regulatory and scientific documents.
- Company: Join Meet Life Sciences, a leader in innovative healthcare solutions.
- Benefits: Enjoy a full-time role with opportunities for remote work and professional growth.
- Why this job: Be part of a dynamic team that values collaboration and continuous learning.
- Qualifications: 5-8 years in medical writing; a degree in life sciences is essential.
- Other info: Mentorship opportunities available for junior writers.
The predicted salary is between 36000 - 60000 £ per year.
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We are seeking an experienced Medical Writing Manager / Lead to oversee the planning, coordination, and delivery of key regulatory and scientific documents. The role involves collaboration with cross-functional teams, management of multiple projects, and a focus on delivering high-quality, compliant documentation.
Main Responsibilities
- Oversee the end-to-end management of medical writing projects, including planning, timeline management, stakeholder coordination, and delivery of final documents.
- Lead the development of a range of documents, including protocol outlines, informed consent forms, clinical study reports, sections of Module 2 of the eCTD, patient-facing materials, lay summaries, registry content, publications, posters, and abstracts.
- Ensure all content is scientifically accurate, clear, and consistent, meeting regulatory and internal quality standards.
- Coordinate with internal teams (clinical, regulatory, biostatistics, data management, patient engagement, project management) and external partners (CROs, KOLs, patient advocacy groups) to gather input and ensure alignment on objectives.
- Conduct quality control checks for accuracy, grammar, formatting, and template compliance across all documents.
- Ensure all documentation complies with applicable regulatory guidelines and company SOPs, and support submission readiness.
- Contribute to process improvement initiatives, including the implementation of AI tools and digital repositories to enhance document development efficiency.
- Maintain accurate records of timelines, milestones, and deliverables, providing regular progress updates to stakeholders.
- Support training and mentoring of junior writers, promoting collaboration and continuous learning within the team.
Requirements
- 5–8 years of medical writing and project management experience in the pharmaceutical, biotech, or related industry.
- Proven experience in a senior or principal medical writing role.
- Bachelor\’s degree in life sciences, pharmacy, or a related field; an advanced degree (e.g. MSc, PhD) is preferred.
- Fluency in English (spoken and written).
- Strong knowledge of scientific and medical terminology, regulatory guidelines, and clinical trial processes.
- Excellent project management, organizational, and communication skills.
- Ability to work independently and collaboratively in a fast-paced, deadline-driven environment.
- Experience mentoring junior team members is a plus.
Seniority level
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Seniority level
Mid-Senior level
Employment type
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Employment type
Full-time
Job function
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Job function
Other
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Manager Medical Writing employer: Meet Life Sciences Ltd.
Contact Detail:
Meet Life Sciences Ltd. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manager Medical Writing
✨Tip Number 1
Network with professionals in the medical writing field. Attend industry conferences or webinars where you can meet potential colleagues and learn about the latest trends. This can help you gain insights into what companies like us are looking for in a candidate.
✨Tip Number 2
Familiarise yourself with regulatory guidelines and standards relevant to medical writing. Understanding these will not only boost your confidence but also demonstrate your commitment to quality and compliance, which is crucial for a role like this at StudySmarter.
✨Tip Number 3
Showcase your project management skills by discussing specific projects you've led in the past. Be prepared to explain how you coordinated with cross-functional teams and managed timelines, as this experience is vital for the Manager Medical Writing position.
✨Tip Number 4
Consider brushing up on your mentoring skills. If you have experience training junior writers, be ready to share examples of how you've supported their development. This will highlight your leadership capabilities, which are essential for this role at StudySmarter.
We think you need these skills to ace Manager Medical Writing
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in medical writing and project management. Emphasise your leadership roles and any specific projects that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your understanding of the role and the company. Mention your experience with regulatory documents and your ability to collaborate with cross-functional teams, as these are key aspects of the position.
Highlight Relevant Skills: In your application, clearly outline your skills in scientific writing, project management, and mentoring. Use specific examples to demonstrate how you've successfully managed similar projects in the past.
Proofread for Quality: Before submitting your application, thoroughly proofread all documents for accuracy, grammar, and formatting. This is crucial in the medical writing field, where attention to detail is paramount.
How to prepare for a job interview at Meet Life Sciences Ltd.
✨Showcase Your Project Management Skills
As a Medical Writing Manager, you'll need to demonstrate your ability to manage multiple projects simultaneously. Be prepared to discuss specific examples of how you've successfully coordinated timelines and stakeholder input in previous roles.
✨Highlight Your Regulatory Knowledge
Make sure to emphasise your understanding of regulatory guidelines and compliance standards. Discuss any experience you have with eCTD submissions or similar documentation processes, as this will be crucial for the role.
✨Demonstrate Collaboration Experience
This position requires working closely with various teams. Share examples of how you've effectively collaborated with clinical, regulatory, and biostatistics teams in the past, and how you ensured alignment on project objectives.
✨Prepare for Quality Control Discussions
Quality is key in medical writing. Be ready to talk about your approach to quality control, including how you check for accuracy, grammar, and formatting in documents. Providing examples of past successes in maintaining high standards will impress your interviewers.
