Overview
At Rieka Talent, we are currently looking for a Clinical Research Associate (CRA) to join an innovative and international company operating within the medical device industry.
This position offers the opportunity to play a key role in clinical investigations, evidence generation, and regulatory documentation within a highly regulated and fast-growing environment.
Position Objective
The CRA will provide clinical and scientific expertise across clinical studies within a medical device environment. This role will be responsible for the clinical investigation lifecycle, including CRO coordination, clinical site identification, site feasibility, investigator engagement, clinical follow-up, and contribution to clinical documentation. The position is critical in ensuring quality, consistency, and regulatory readiness of clinical evidence, supporting informed decision-making and compliance throughout the medical device lifecycle.
Key Responsibilities
- Clinical Studies: Design, plan, coordinate, and oversee clinical investigations for medical devices in compliance with EU MDR (2017/745),



ISO 14155, and applicable regulations
- Identify and coordinate clinical investigation sites and investigators
- Conduct feasibility assessments and maintain site follow-up activities
- Act as the main point of contact for CROs, investigators, and clinical sites
- Draft clinical study protocols and essential clinical documentation
- Coordinate collection, review, and consolidation of clinical data ensuring quality and traceability

Clinical Documentation
Preparation and maintenance of clinical sections of Technical Documentation, including:
- Clinical Evaluation Plan (CEP)
- Clinical Evaluation Report (CER)
- Clinical Development Plan (CDP)

What the Company Offers
- Hybrid working model
- International and collaborative environment
- Opportunity to join a growing and innovative company
- Exposure to general clinical projects within the medical device sector
- High visibility and di

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