Role

Data Entry / Study Coordinator

Join Pratia and help shape the future of clinical research.

At Pratia, we believe that patients should have access to innovative treatments that can change their lives. We are one of the largest international networks of clinical research centres, with over 90 centres across Europe and the United States, working every day to bring clinical trials and cutting-edge therapies to patients and healthcare professionals.

Our mission is to expand access to innovative therapies, both in oncology and other therapeutic areas, whilst always ensuring the highest standards of quality, safety and patient care. Since 2012, we have conducted more than 3,000 clinical trials and have earned the trust of more than 300,000 patients and 1,000 doctors worldwide.

We are currently looking for several Data Entry / Study Coordinators to join our team and play a key role in the management and conduct of clinical trials at the site level in Madrid

What will your role involve?

As a Data Entry / Study Coordinator, you will play a key role in the conduct of clinical trials, working closely with the research team and sponsors throughout the entire study lifecycle. Your main responsibilities will include:

✅ Coordinating the activities of the clinical trial.

✅ Managing and maintaining the study documentation and records.

✅ Entering and reviewing data in the trial’s electronic systems (eCRF).

✅ Managing and resolving queries

✅ Providing support during monitoring visits,



audits and inspections.

✅ Ensuring compliance with applicable procedures and regulations.

✅ Coordinating the dispatch and management of biological samples.

✅ Collaborating with investigators, CRAs, sponsors and other professionals involved in the study.

What are we looking for?

Requirements

✔ A university degree in Health Sciences, Nursing, Pharmacy, Biology, Medicine or a related discipline.

✔ Previous experience in clinical research or similar roles within the healthcare sector. Minimum 6 months (work placements count as experience)

✔ English language proficiency at B2 level or above.

✔ Strong organisational skills and the ability to prioritise.

✔ Attention to detail and a focus on quality.

✔ Communication and teamwork skills.

✔ A proactive attitude and a patient-centred approach.

We will view the following as a plus:

➕ Specific training in clinical research.

➕ Knowledge of Good Clinical Practice (ICH-GCP) and the regulations applicable to clinical trials.

Why join Pratia?

✨ Be part of a leading international network in clinical research.

✨ Contribute directly to patients’ access to innovative treatments.

✨ Work alongside professionals with extensive experience in clinical research.

✨ Take part in studies across different therapeutic areas and innovative projects.

✨ Enjoy a collaborative, dynamic environment focused on professional development.

📌 Data Entry / Study Coordinator (Madrid)
🏢 Humaneva Group
📍 Madrid