Gestor/a de Investigación Clínica

• Familiarity with Good Clinical Practice (ICH-GCP) and applicable clinical research regulations.
• Good English level & high communication skills (written & oral).
• Good organizational skills, excellent attention to detail and ability to plan and organize work.
• High level of initiative, self-motivation capacity and ability to work in a multidisciplinary team.
• Ability to interact confidently with investigators, healthcare professionals and other units.

• Experience in RedCAP databases/CRD design and management is desirable.
• Complementary training/experience on clinical studies/trials management, including writing of clinical protocols and informed consent forms, will be appreciated.
• Previous experience in participant recruitment, study coordination and clinical research activities will be highly valued.
• Experience as a Clinical Research Coordinator, CRA or in a similar clinical research role will be valued.
• Writing skills, creativity and ability in design will be an asset.

Education and field of expertise

Degree in Health Sciences. An MD is highly desirable, and a PhD will be considered an asset.

• Degree in Health Sciences. An MD is highly desirable, and a PhD will be considered an asset.

Spanish and English (mandatory); Catalan (highly desirable)

In liaison with the head of the CMU and her team, the successful candidate will:

IrsiCaixa, located at Hospital Germans Trias i Pujol, has an open position for a Clinical Research Manager. The role aims to strengthen the Clinical Management Unit team. IrsiCaixa have been actively involved in research related to infectious diseases, immune system disorders, and emerging viruses like COVID-19. Furthermore, IrsiCaixa conducts clinical studies to contribute with knowledge and to improve patients' quality of life. This unit is dedicated to ensuring compliance with current regulations regarding clinical studies, including sample and data protection. Additionally, it closely assists the researchers at IrsiCaixa in preparing all necessary documentation and performing all required tasks.

• Assist researchers in the management and coordination of clinical studies.
• Support in clinical protocols and informed consents development.
• Support on design/creation of study databases and EDCs (including REDCap).
• Organization and preparation of the required materials necessary to implement to the projects.
• Screening, selection and classification of samples/candidates for studies.
• Interaction with investigators, clinical staff and study participants.
• Medical review and follow-up of study-related clinical documentation, when applicable.
• Organization/attendance to meetings, presentations & minutes.

Oferta de trabajo

Gestor/a de investigación clínica Ver todos las ofertas

1. Inicio
2. Carrera científica
3. Trabaja con nosotros
4. Gestor/a de investigación clínica

Side1

Full/part time

Full time

Job code

Starting date

September 8, 2026

Application deadline

Opened until the position is covered. 1st review of applications will take place on the 31st of August

Side2

Field

Clinical Management Unit (CMU)

Direct supervisor

Head of the CMU

Experience

Minimum 2 years of experience in clinical research, preferably in the coordination and management of clinical studies or clinical trials

Languages

Documento

GEST-CMU_01_072026.pdf

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Summary

Job duties

Candidate profile and qualifications

What we offer

Required documents

• Cover letter
• Resume (CV)
• Recommendation letter (optional but appreciated)
• Other relevant documents

Selection process

Where to find us

Form