Senior Clinical Trial Administrator en Málaga, España - Jobeax
Descripción de la vacante
Senior Clinical Trial Administrator en Málaga, España
MDx CRO
RemotoTrabaja desde cualquier lugar
Tiempo completoJornada semanal estándar
ContratoTemporal o freelance
Spain, Málaga
Senior Clinical Trial Administrator en Málaga, España is listed on Jobeax. Browse 80,000+ vacancies available.
Clinical Research and Regulatory Specialist | MedTech Location: 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. Ideal 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 and continuous training
Close mentorship from senior specialists
Exposure to real clinical and scientific projects
MDx CRO is a leading Contract Research Organisation specialising in in vitro diagnostics (IVDs) and medical devices. We provide regulatory consulting, clinical research, and quality assurance services, helping clients bring safe and effective products to market in full compliance with global regulatory standards.
We pioneer emerging technologies and navigate uncharted territories to redefine the future of the medical sector.
If you want to accelerate your development in the MedTech and IVD sector within a supportive and expert‑driven environment, we would love to hear from you.
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