At a Glance
- Tasks: Create clinical study reports and collaborate with project teams in oncology trials.
- Company: Join Cancer Research UK, a leader in cancer research and innovation.
- Benefits: Flexible hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Enjoy a supportive environment with minimal travel and a focus on collaboration.
- Why this job: Make a difference in cancer research while developing your writing and project management skills.
- Qualifications: Strong medical writing background and a science degree required.
The predicted salary is between 40000 - 50000 £ per year.
Cancer Research UK (CRUK) is seeking a Regulatory Medical Writer to support its platform trial, DETERMINE. This full-time, 24-month fixed-term role allows for flexible home-based working with minimal travel requirements.
You will produce clinical study reports and liaise with project teams, making collaboration essential.
The ideal candidate will have a strong background in medical writing and a science degree, along with excellent proofreading and project management skills.
Regulatory Medical Writer – Oncology Trials (Hybrid) employer: Cancer Research UK (CRUK)
Cancer Research UK offers a dynamic and supportive work environment for Regulatory Medical Writers, particularly in the field of oncology trials. With a strong emphasis on collaboration and flexibility, employees benefit from a hybrid working model that promotes work-life balance while contributing to groundbreaking cancer research. The organisation prioritises professional development, providing ample opportunities for growth and advancement within a mission-driven culture dedicated to making a meaningful impact in the fight against cancer.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Medical Writer – Oncology Trials (Hybrid)
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry events. A friendly chat can open doors and give you insights into the role that might not be in the job description.
✨Tip Number 2
Show off your skills! Prepare a portfolio of your best medical writing samples, especially those related to clinical studies. This will help you stand out during interviews and demonstrate your expertise.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers. Focus on how your experience aligns with the needs of CRUK and the DETERMINE trial.
✨Tip Number 4
Apply through our website! We love seeing candidates who take the initiative. It shows you're genuinely interested in the role and helps us keep track of your application more easily.
We think you need these skills to ace Regulatory Medical Writer – Oncology Trials (Hybrid)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in medical writing and oncology trials. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about cancer research and how your skills can contribute to our DETERMINE trial. Keep it engaging and personal.
Showcase Your Collaboration Skills:Since collaboration is key for this role, mention any experiences where you’ve worked closely with project teams. We love seeing examples of teamwork and communication in action!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Cancer Research UK (CRUK)
✨Know Your Stuff
Make sure you brush up on your medical writing skills, especially in the context of oncology trials. Familiarise yourself with clinical study reports and the specific requirements for regulatory submissions. This will show that you're not just a good writer, but also someone who understands the nuances of the field.
✨Showcase Your Collaboration Skills
Since this role involves liaising with project teams, be prepared to discuss your experience working collaboratively. Think of examples where you've successfully worked with others to achieve a common goal, particularly in a scientific or medical context. This will highlight your ability to fit into their team dynamic.
✨Prepare for Project Management Questions
Given the importance of project management in this role, anticipate questions about how you handle deadlines and manage multiple projects. Have specific examples ready that demonstrate your organisational skills and ability to prioritise tasks effectively.
✨Proofreading is Key
As a Regulatory Medical Writer, attention to detail is crucial. Be ready to discuss your proofreading process and any tools or techniques you use to ensure accuracy. You might even want to bring a sample of your work to showcase your meticulousness and writing style.
