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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; advanced degree preferred.
- Other info: Mentorship opportunities available for junior writers.
The predicted salary is between 43200 - 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 expertise but also demonstrate your commitment to staying updated in this fast-paced field.
✨Tip Number 3
Showcase your project management skills by discussing specific examples of how you've led cross-functional teams in previous roles. Highlighting your ability to manage timelines and deliverables will make you stand out.
✨Tip Number 4
Prepare for interviews by reviewing common questions related to medical writing and regulatory submissions. Practising your responses will help you articulate your experience and skills effectively during discussions with our team.
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: Write a cover letter that showcases your understanding of clinical data and regulatory requirements. Mention specific examples of documents you have developed, such as Investigators' Brochures or Clinical Study Reports, to demonstrate your expertise.
Highlight Leadership Experience: Since the role involves mentoring junior writers and leading cross-functional teams, be sure to include any leadership roles you've held. Discuss how you've contributed to process improvements or guided teams in previous positions.
Showcase Communication Skills: Given the importance of communication in this role, provide examples of how you've effectively interacted with team members and senior leaders. This could include experiences from meetings or collaborative projects that required strong interpersonal skills.
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 readiness 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.
