About this role:

Your responsibilities:

• Get authorised to assess the clinical evaluation processes of medical devices.
• Collaborate with a multidisciplinary team on technical documentation assessments.
• Create content to explain complex regulatory topics to customers and prospects.
• Screen and action regulatory insights from the latest research, standards and guidance.
• Support Sales and Customer Experience with regulatory insights on prospects and customers.
• Work with Product, Engineering, Design and Applied ML teams to build and improve systems.
• Support Technical Operations as Scarlet expands approvals in different jurisdictions and technologies.

The key skills:

• Degree in clinical medicine, nursing, radiography, medical physics, biomedical engineering, or related discipline.
• Minimum two years' experience in patient care, clinical imaging, radiology operations, or related healthcare practice.
• Experience using medical device software or non-implantable imaging devices utilising ionising radiation (e.g. CT, gamma cameras, fluoroscopy, PET).
• Minimum two years' experience assessing clinical data for medical devices.
• Knowledge of principles for assessing clinical data and medical statistics.
• Practical experience conducting or monitoring clinical investigations/trials or assessing clinical data.

Desirable skills:

• Research savvy with knowledge of clinical research methodologies and trial design.
• Excellent written and verbal communication skills.
• Highly adaptable and able to operate with autonomy in ambiguous situations.
• Knowledge or training in relevant standards and guidance for clinical evaluation (e.g. ISO 14155, MEDDEV 2-7/1 Rev.4).

The 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 - 2x30 mins
• Referencing and offer