About MammoCheck
MammoCheck Ltd is a Cyprus-based medical technology company and a Frederick University spin-out. We are developing an AI-powered Software as a Medical Device (SaMD) for adjunctive breast cancer screening. Our solution pairs consumer thermal imaging hardware with a proprietary deep learning model, delivered through a smartphone application, and is designed to support rather than replace clinical judgement. The product is positioned strictly as adjunctive and investigational while we advance toward FDA 510(k) clearance and CE marking under the EU Medical Device Regulation (EU MDR). We are now building the in-house regulatory and quality capability that will carry the product through clinical validation, regulatory submission, and market entry.
Role overview
As Research Assistant, you will be at the heart of MammoCheck's clinical study, responsible for collecting thermal images at our partner clinics across Cyprus and preparing the resulting datasets for research use. You will work on site with clinicians and study participants, operate the thermal imaging equipment according to the approved study protocol, and then organise, quality-check, and pseudonymise the data so it is ready for the research team. You will be trained on the study protocol, Good Clinical Practice basics, and data protection procedures, and you will be supported throughout by the clinical team, the management team, and the technical team. This is a meaningful, patient-facing role in a study approved by the Cyprus National Bioethics Committee.
What you will implement
- Conduct thermal image acquisition sessions at partner clinics across Cyprus, following the approved study protocol exactly and working alongside clinic staff.
- Set up, operate, and care for the thermal imaging equipment, and keep calibration and session logs.
- Support study participants through the imaging session with professionalism, sensitivity, and respect for privacy and dignity at all times.
- Perform quality checks on captured images at the point of collection, flagging and repeating substandard captures according to protocol.
- Prepare datasets for research use: organise, label, pseudonymise, and securely transfer images and session metadata following the Company's data protection procedures.
- Maintain accurate collection records, participant session documentation, and chain-of-custody logs for the study.
- Coordinate scheduling with clinic staff and report progress, issues, and protocol deviations promptly to the clinical and management teams.
Guidance, training, and support
You will not be doing this alone. Strategy and specialist judgement are provided by our external consultants, who will train you on the frameworks, review your work, and remain available throughout. The management team provides direction and removes blockers, and the technical team supplies the engineering inputs and tooling you need. Your job is to implement, own the day-to-day system, and grow into the expert in the room.
Required qualifications
- A degree or diploma in biomedical science, health sciences, nursing, radiography, computer science, or a related field, or equivalent experience in a clinical or research setting.
- Fluent Greek and good English. The role is participant-facing in Cyprus clinics, so Greek is essential.
- Exceptional attention to detail and reliability. Protocol adherence and data quality are the core of this role.
- Professionalism, discretion, and sensitivity when working with study participants in a screening context.
- A valid driving licence and willingness to travel between clinic sites across Cyprus.
- Comfort with technology: operating imaging equipment, tablets, and data management tools. Full training is provided.
Preferred qualifications
- Experience in a clinical, laboratory, or research data collection setting.
- Familiarity with Good Clinical Practice or research ethics requirements.
- Experience with data organisation, spreadsheets, or basic scripting.
- Prior work with medical imaging of any modality.
What we offer
- A competitive salary.
- Structured guidance and training from our external regulatory and quality consultants and specialist FDA and EU MDR advisors.
- Direct support from the management team and the technical team, so you are never implementing alone.
- Support for professional development and certification, including RAPS and ISO 13485 training.
- Flexible and hybrid working arrangements.
- A front-row role in a bioethics-approved clinical study, with training in Good Clinical Practice, data protection, and medical imaging research workflows.
How to apply
To apply, please send your CV and a short cover letter to [email protected] with the role title in the subject line, or apply directly using the form below. Applications are reviewed on a rolling basis.