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- Tasks: Lead the creation of clinical documents for global regulatory submissions in oncology.
- Company: Join a leading global pharmaceutical company focused on innovative oncology solutions.
- Benefits: Enjoy remote work flexibility and opportunities for professional growth.
- Why this job: Make a real impact in healthcare while collaborating with talented professionals.
- Qualifications: Requires 7+ years in medical writing and a relevant degree; advanced degree preferred.
- Other info: Mentorship opportunities available for junior writers and involvement in process improvements.
The predicted salary is between 48000 - 72000 £ per year.
Remote Associate Director, Principal Medical Writer working through an FSP model for a Global Oncology focused Pharmaceutical Company
The Associate Director, Principal Medical Writer is responsible for developing clinical documents for regulatory submissions worldwide. This role involves leading cross-functional project teams to ensure documents—such as Investigators\’ Brochures (IBs) and Clinical Study Reports (CSRs)—accurately present clinical data in line with regulatory requirements.
Key Responsibilities:
- Write or supervise the writing of high-quality, scientifically rigorous documents. –
- Oversee medical writing for multiple compounds and lead regulatory submissions. – Participate in cross-functional meetings to discuss medical writing deliverables and timelines.
- -Review relevant project documents, such as Protocols and Statistical Analysis Plans. –
- Mentor junior writers and contribute to process improvement initiatives.
Qualifications:
- A bachelor’s degree is required; an advanced degree is preferred.
- Minimum 7 years of medical writing experience in the biopharmaceutical or CRO industry.
- Strong ability to understand and interpret clinical data, with excellent project management skills. – Strong verbal, written, and interpersonal communication skills. –
- Knowledge of global regulatory requirements and therapeutic areas in clinical development.
- Proficiency in MS Word and experience with electronic document management systems is essential.
- This position requires effective interaction with team members and senior leaders to facilitate communication and problem-solving.
Associate Director, Principal Medical Writer employer: Advanced Clinical
Contact Detail:
Advanced Clinical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Principal Medical Writer
✨Tip Number 1
Network with professionals in the biopharmaceutical and CRO industries. Attend relevant conferences or webinars to connect with others in medical writing and oncology, as personal connections can often lead to job opportunities.
✨Tip Number 2
Familiarise yourself with the latest global regulatory requirements and guidelines in clinical development. This knowledge will not only enhance your understanding but also demonstrate your commitment to staying current in the field during interviews.
✨Tip Number 3
Prepare to discuss specific examples of your project management experience and how you've led cross-functional teams. Highlighting your leadership skills and ability to mentor junior writers will set you apart from other candidates.
✨Tip Number 4
Showcase your proficiency in MS Word and any electronic document management systems you've used. Being able to discuss your technical skills confidently can give you an edge, especially in a role that requires high-quality document preparation.
We think you need these skills to ace Associate Director, Principal Medical Writer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your medical writing experience, especially in the biopharmaceutical or CRO industry. Emphasise your project management skills and any relevant qualifications that align with the job description.
Craft a Compelling Cover Letter: In your cover letter, explain why you are a great fit for the Associate Director, Principal Medical Writer role. Mention specific experiences that demonstrate your ability to lead cross-functional teams and your understanding of regulatory requirements.
Showcase Your Writing Skills: Include samples of your previous work, such as clinical documents or reports, to showcase your writing style and ability to present complex data clearly. Ensure these samples reflect high-quality, scientifically rigorous writing.
Highlight Leadership Experience: Since the role involves mentoring junior writers and leading projects, be sure to highlight any leadership roles you've held. Discuss how you've contributed to process improvements and team success in your previous positions.
How to prepare for a job interview at Advanced Clinical
✨Showcase Your Writing Skills
As a Principal Medical Writer, your writing ability is crucial. Bring samples of your previous work to the interview, and be prepared to discuss your writing process and how you ensure scientific rigor in your documents.
✨Demonstrate Project Management Expertise
Highlight your project management skills by discussing specific examples where you've led cross-functional teams or managed multiple projects simultaneously. This will show your potential employer that you can handle the responsibilities of overseeing medical writing for various compounds.
✨Familiarise Yourself with Regulatory Requirements
Since this role involves regulatory submissions, brush up on global regulatory requirements relevant to oncology. Being able to discuss these during the interview will demonstrate your knowledge and preparedness for the position.
✨Prepare for Team Interaction Scenarios
Expect questions about how you interact with team members and senior leaders. Prepare examples of how you've facilitated communication and problem-solving in past roles, as this is key to succeeding in a collaborative environment.
