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For Companies At a Glance
- Tasks: Lead clinical research and generate evidence for innovative medical devices.
- Company: Join TidalSense, a pioneering company in medical technology.
- Benefits: Competitive salary, flexible hours, hybrid work, and generous leave.
- Why this job: Make a real impact in healthcare while developing your skills.
- Qualifications: Bachelor's in a scientific field and experience in clinical research.
- Other info: Dynamic team culture with excellent growth opportunities and mental health support.
The predicted salary is between 34000 - 63000 £ per year.
Job Purpose: To take a leading role in the generation of clinical evidence and scientific content to support the regulation, scientific profile, and adoption of TidalSense's medical devices.
Key Duties & Responsibilities
- Clinical research: Contribute to the creation and development of the company's global clinical evidence strategy. Design, plan and project manage research programmes. Write project charters, study protocols and ethics submissions and other required study documentation. Contribute to and oversee study implementation, monitoring and close out, including site visits, formal study reporting and registrations, and communications with external stakeholders (e.g. MHRA, grant monitoring officers). Critically analyse current clinical processes, and design/implement process improvements to optimise efficiency and delivery of targets.
- Scientific writing: Write, review and edit clinical scientific content, including peer-reviewed scientific publications, conference abstracts, white papers, scientific and clinical marketing content, product manuals and educational materials. Support with writing grant applications for (clinical) research programmes.
- Stakeholder management: Work closely with the clinical, commercial and marketing teams to support key clinical stakeholder management, including building and maintaining a network of key opinion leaders to support current and future studies.
- Clinical evaluation and regulatory: With support from the rest of the clinical team, take a leading role in the planning and execution of clinical evaluation in accordance with EU MDR and other applicable regulatory requirements for existing and new medical devices, including writing and reviewing Clinical Evaluation Plans and Reports and Post-Market Clinical Follow-up Plans and Reports. Planning, running and reporting systematic literature searches.
Requirements & Skills & Competencies
- Excellent written and verbal communication skills; with the ability to describe complex scientific concepts for diverse audiences.
- Strong analytical and research skills, including the ability to conduct systematic literature searches, design studies, and interpret data.
- Strong organisational, risk management and project management skills.
- Ability to deliver to deadlines, comfortable with uneven workloads.
- Excellent verbal communication and people skills.
- Views Generative AI and automation tools as a 'force multiplier' for their own productivity and is eager to pioneer new workflows in a regulated healthcare environment.
- Attention to detail.
- Willingness to learn and develop processes and personal skills.
- Strong team spirit and hands-on mentality.
Qualifications & Experience
- Essential: Bachelor's degree in a scientific or clinical subject. Experience in scientific writing, including publication of articles in peer-reviewed journals and managing publications through the peer review process. Experience of designing, managing or contributing to clinical research projects. Experience of project management.
- Desirable: Qualified healthcare professional (e.g. doctor, nurse or other allied health professional). PhD or DPhil in a scientific or clinical subject. Experience of protocol/bid/grant writing. Experience of medical statistics and/or health economics. Experience working within a quality management system (preferably ISO 13485 or ISO 9001). Experience working with medical device products.
Other Requirements
- Legally eligible to work in the UK without sponsorship. Please note that we are open to sponsoring colleagues to move from an unsponsored visa to a Skilled Worker Visa once they have passed their probation.
- Will need to be able to work in person in the Cambridge office at least 3 days/week (but ideally more).
Note to Applicants
We read all applications carefully - including your free-text answers - in evaluating your application. Please make sure you spend some time answering these questions carefully. Please answer questions truthfully and without using a LLM to auto-populate answers. Dishonesty is fundamentally against our values. We appreciate that some candidates may hesitate to apply because they may feel that they might not meet all of the required criteria or be competitive enough. If this is you, please don’t shy away from applying - we would like to hear from you!
Closing date for applications: Sunday 22nd February 2026
Benefits
- Salary £40,000-75,000 (depending on experience).
- Flexible working hours to support your work preferences.
- Hybrid working as per requirements above.
- 25 days annual leave (pro-rated) + 8 public holidays.
- Pension: TidalSense contributes 5% of qualified earnings.
- Annual performance-based bonus.
- Discretionary share options scheme.
- Work from abroad for 1 week per year.
- Buy/sell up to 5 days annual leave (pro-rated).
- Individual personal development budget + dedicated development days.
- Mental Health support: wellbeing support and free 24/7 access to qualified counsellors and advisors.
- Coaching and mentoring.
- Team events and celebrations.
- Beautiful award-winning Cambridge UK office stocked with quality drinks & snacks.
Clinical Scientist in Cambridge employer: TidalSense
Contact Detail:
TidalSense Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Scientist in Cambridge
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical field on LinkedIn or at industry events. Building connections can lead to job opportunities that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to clinical research. We recommend doing mock interviews with friends or mentors to boost your confidence.
✨Tip Number 3
Showcase your skills through a portfolio! If you've worked on any relevant projects, compile them into a neat presentation. This can really set you apart during interviews.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love hearing from passionate candidates like you!
We think you need these skills to ace Clinical Scientist in Cambridge
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your application to highlight how your skills and experiences align with the role of Clinical Scientist. We want to see how you can contribute to our clinical evidence strategy and scientific content creation.
Show Off Your Writing Skills: Since this role involves a lot of scientific writing, include examples of your previous work. Whether it’s peer-reviewed articles or project charters, we love seeing your ability to communicate complex ideas clearly.
Be Honest and Authentic: When answering our application questions, be truthful and genuine. We appreciate candidates who are open about their experiences and skills, so don’t hesitate to share your journey with us!
Apply Through Our Website: We encourage you to submit your application through our website. It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at TidalSense
✨Know Your Clinical Evidence Strategy
Before the interview, dive deep into TidalSense's clinical evidence strategy. Familiarise yourself with their medical devices and how they align with current regulations. This will not only show your interest but also your understanding of the role's significance in supporting the company's objectives.
✨Showcase Your Scientific Writing Skills
Prepare to discuss your experience in scientific writing. Bring examples of your published articles or any relevant documentation you've worked on. Being able to articulate complex scientific concepts clearly is crucial, so practice explaining these in layman's terms as well.
✨Demonstrate Project Management Prowess
Be ready to talk about your project management experience. Highlight specific projects where you designed, managed, or contributed significantly. Use the STAR method (Situation, Task, Action, Result) to structure your responses and showcase your organisational skills.
✨Engage with Stakeholder Management
Since stakeholder management is key in this role, think of examples where you've successfully built relationships with key opinion leaders or external stakeholders. Discuss how you maintained these connections and the impact they had on your projects.
