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For Companies At a Glance
- Tasks: Generate clinical evidence and write scientific content for regulatory approval.
- Company: Leading medical devices company based in Cambridge with a focus on innovation.
- Benefits: Flexible hours, mental health support, and competitive salary ranging from £40,000-75,000.
- Why this job: Make a real impact in healthcare by supporting product adoption and regulatory success.
- Qualifications: Degree in a scientific field and experience in scientific writing and project management.
- Other info: Collaborative environment with opportunities for professional growth.
The predicted salary is between 40000 - 75000 £ per year.
A medical devices company in Cambridge seeks a Clinical Evidence Specialist to generate clinical evidence and scientific content to support regulatory approval and market adoption of their products. The role includes writing scientific publications, managing clinical research projects, and collaborating closely with various teams to ensure successful stakeholder management.
Essential qualifications include a degree in a scientific field and experience in scientific writing and project management.
The salary range is £40,000-75,000 with various benefits including flexible hours and mental health support.
Clinical Scientist: Evidence & Regulation Lead (Hybrid) in Cambridge employer: TidalSense
Contact Detail:
TidalSense Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Scientist: Evidence & Regulation Lead (Hybrid) in Cambridge
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical devices field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions related to clinical evidence and project management. We recommend doing mock interviews with friends or using online platforms to boost your confidence.
✨Tip Number 3
Showcase your scientific writing skills! Bring along samples of your work to interviews or share them in your portfolio. This will help us see your expertise in generating clinical evidence and scientific content.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Clinical Scientist: Evidence & Regulation Lead (Hybrid) in Cambridge
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Scientist role. Highlight your experience in scientific writing and project management, as these are key for us. Use specific examples that showcase your skills and achievements.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Tell us why you're passionate about clinical evidence and how your background makes you a perfect fit for the team. Keep it engaging and relevant to the job description.
Showcase Your Scientific Writing Skills: Since writing scientific publications is part of the role, include samples or links to your previous work if possible. This will give us a taste of your writing style and expertise in generating clinical evidence.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at TidalSense
✨Know Your Science
Make sure you brush up on the latest developments in clinical evidence and regulatory processes. Being able to discuss recent publications or advancements in medical devices will show your passion and expertise in the field.
✨Showcase Your Writing Skills
Since scientific writing is a key part of the role, prepare a portfolio of your previous work. Bring examples of publications or reports you've authored, and be ready to discuss your writing process and how you tailor content for different audiences.
✨Project Management Prowess
Be prepared to talk about your experience managing clinical research projects. Highlight specific challenges you faced, how you overcame them, and the outcomes. This will demonstrate your ability to handle the responsibilities of the role effectively.
✨Collaboration is Key
This role involves working closely with various teams, so be ready to discuss your experience in stakeholder management. Share examples of how you've successfully collaborated with cross-functional teams to achieve project goals.
