At a Glance
- Tasks: Join a dynamic team assessing innovative medical devices and ensuring regulatory compliance.
- Company: Scarlet, a forward-thinking company revolutionising medical technology.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and career development.
- Why this job: Make a real impact in healthcare by evaluating cutting-edge medical technologies.
- Qualifications: Degree in clinical medicine or related field with relevant experience in healthcare.
The predicted salary is between 50000 - 65000 £ per year.
Scarlet pulls medical technology from the future to solve human health. Authorised by governments around the world to assess medical AI, we remove unnecessary delays from every regulatory approval so patients get devices from the future, today. We are proud to count the world’s most ambitious companies building medical technology as customers. You will be joining a team with product‑market fit, flowing data, and exponentially growing revenue.
ABOUT THIS ROLE
Scarlet’s Devices function is a team of clinicians, AI experts, and software engineers, working together to assess and certify the most innovative and impactful medical device software. We pride ourselves on delivering fast and efficient assessments to enable market access, new device updates, and ongoing surveillance of a growing portfolio of medical devices. As we continue to scale our activities and certify more medical devices, we need clinical and regulatory expertise to provide support across all stages of the customer journey. You’ll join a team of clinical evaluation experts, conducting swift and accurate device assessments, whilst providing knowledge and expertise to internal functions and external stakeholders.
YOUR RESPONSIBILITIES
- Get authorised to assess the clinical evaluation processes of the most innovative medical devices in the world.
- Collaborate with a multidisciplinary team on technical documentation assessments.
- Create content to help explain complex regulatory topics to customers and prospects.
- Screen and action regulatory insights from the latest research, standards, and guidance.
- Support the Sales and Customer Experience function by providing regulatory insights on prospects and customers.
- Work with our Product, Engineering, Design, and Applied ML functions to build and improve our systems.
- Support the Technical Operations function as they expand Scarlet’s approvals in various jurisdictions and technologies.
KEY SKILLS
- Education – A degree in clinical medicine, nursing, radiography, medical physics, biomedical engineering, or a related discipline.
- Work experience – Minimum of two years experience in patient care, clinical imaging, radiology operations, or related healthcare practice.
- Work experience – Experience using medical device software or active non‑implantable imaging devices utilising ionising radiation (e.g. X‑ray computer tomography, gamma cameras, fluoroscopy, PET scanners).
- Work experience – Minimum of two years experience with the assessment of clinical data for medical devices.
- Work experience – Knowledge of the fundamental principles of the assessment of clinical data for medical devices and medical statistics.
- Work experience – Practical experience in conducting or monitoring clinical investigations/trials or assessing clinical data.
DESIRABLE SKILLS
- Ferociously curious – You like going down rabbit holes, understanding deeply how things work, and challenging the status quo.
- Research savvy – You have knowledge of different clinical research methodologies, including experience designing or contributing to the development of clinical trials.
- Excellent communicator – You have exceptional written & verbal communication skills.
- Highly adaptable – You have worked in different environments and like operating with autonomy on sometimes ambiguous tasks.
- Guidance knowledge – You have knowledge or training in the relevant standards and guidance used for clinical evaluation (e.g. ISO 14155, MEDDEV 2‑7/1 Rev. 4).
INTERVIEW PROCESS
- Intro call with Kim – 20 mins.
- Interview with Sandy – 45 mins.
- Technical interview with Kim – 1 hour.
- Culture and values interview with James and Jamie – 2 × 30 mins.
- Referencing & offer.
Clinical Evaluation Specialist - Radiology London employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
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We think this is how you could land Clinical Evaluation Specialist - Radiology London
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How to prepare for a job interview at Meeveem Limited
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