Clinical Research and Regulatory Specialist | MedTech 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.

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 (Castro)
🏢 MDx CRO
📍 Castro