Clinical Research and Regulatory Specialist | MedTech Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación.

Location: Spain (Remote)

Employment type: Full-time

Role Summary

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.

Responsibilities

You will

Support the preparation and execution of Clinical Investigations and Performance Studies

Assist in developing study documentation (protocols, CRFs, ICFs)

Collaborate with study sites and internal teams following ISO 14155 and ISO 20916 standards

Handle study documentation and communication with investigators

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

You will receive structured onboarding, mentoring, and progressive responsibility.

You are not expected to know everything on day one — you will learn with us.

Requirements (Must‐Have)





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

Motivation to grow in a dynamic and international environment

Availability for remote work with occasional in‐person activities

Nice to Have

Exposure to ISO 14155 or ISO 20916

R&D; experience

Regulatory exposure

Academic research experience or authorship in scientific literature

Why Join MDx CRO

At MDx CRO, you will join a dynamic and rapidly growing company recognised across the MedTech and IVD industry.

We offer

Structured onboarding and continuous training

Close mentorship from senior specialists

Exposure to real clinical and scientific projects

Growth opportunities as your skills develop

About MDx CRO

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 general regulatory standards. xiphteb

We operate on five core principles:

Make it POSSIBLE

Make it WIN-WIN

Keep IMPROVING

Keep GROWING

Keep it DIVERSE

Our Vision To democratise access to world-class regulatory and clinical strategies, ensuring safer and more effective medical technologies for all.

Our Mission

We pioneer emerging technologies and navigate uncharted territories to redefine the future of the medical sector.

Grow with Us

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.

📌 Clinical Research Specialist | MedTech (Tabagón)
🏢 MDx CRO
📍 Tabagón