Clinical Research and Regulatory Specialist | MedTech Se anima a todos los posibles solicitantes a que se desplacen y lean la descripción completa del puesto antes de presentar su candidatura.
Spain (Remote)
Full-time
We are looking for a motivated junior professional who wants to develop their career in the MedTech and IVD sector.
As a Clinical Research and Regulatory Specialist, you will support clinical research activities, scientific and medical writing, and the creation of documentation essential to product validation and regulatory pathways.
You will work closely with senior experts and multidisciplinary teams, gaining hands-on experience with clinical investigations, performance studies (ISO 14155 and ISO 20916), technical documentation, and clinical evidence development.
Idóneo for candidates with 0.5–2 years of experience in MedTech, IVD, clinical research or R&D; — or strong scientific backgrounds eager to enter the industry.
Support the preparation and execution of Clinical Investigations and Performance Studies




Assist with monitoring‐support activities and data‐related tasks
Contribute to scientific and medical writing, including study summaries and evidence-based content
Support literature reviews, background research, and documentation preparation
Assist in drafting components of clinical evidence documentation under supervision
Help coordinate project activities, timelines, and communication
Based in Spain or eligible for a Spanish employment contract
0.5–2 years of experience in MedTech, IVD, clinical research, or R&D;
Strong interest in MedTech, IVDs, clinical research, and scientific development
Bachelor's degree in Life Sciences
Enrolment in or completion of a Master's degree in Life Sciences
Knowledge of GCP and clinical/lab standards
Advanced English (C1–C2), especially for scientific writing
Availability for remote work with occasional in‐person activities
Academic research experience or authorship in scientific literature
Structured onboarding an

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