Gestor/a de Investigación Clínica

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

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

Education and field of expertise

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

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Summary

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.

Job duties

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

• 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.

Candidate profile and qualifications

• Degree in Health Sciences. An MD is highly desirable, and a PhD will be considered an asset.
• 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.
• Familiarity with Good Clinical Practice (ICH-GCP) and applicable clinical research regulations.
• Writing skills, creativity and ability in design will be an asset.
• 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.

What we offer

We are a leading research center in infectious diseases and immunity committed to excellence and innovation. We engage in pioneering projects that have a significant impact on advancing knowledge and improving the quality of life. We value diversity and, as such, encourage and welcome applications from individuals of all genders, nationalities, skin colors, origins, religions and ideologies, ages, sexual orientations, and identities. Moreover, we offer:

• A dynamic and highly collaborative unit.
• An international and interdisciplinary research environment consisting of wet lab scientists and data analysts.
• Versatile activity. Mixed basic and clinical research environment in biomedicine.
• Extensive opportunities for further education & training as well as an excellent working atmosphere in a friendly, committed team.
• Flexible working hours and the compatibility of career and family.
• Hybrid work model (on-site + teleworking) subject to the foundation's regulations.
• State-of-the-art infrastructures & well-equipped offices/relaxing areas; subsidized cafeteria.
• Generous vacation package: 22 vacation days, plus 4 days at Christmas, Holy Thursday, 5 institutionally designated non-working afternoons, and 3 discretionary days (subject to each year's calendar).
• Intensive work schedule: every Friday throughout the year, and during July and August.
• Salary will depend on skills/experience and will be in accordance with IrsiCaixa's salary scales.

Required documents

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

Selection process

• Candidates' documents compilation
• Preselection of candidates and interviews
• Communication of the selection result to the candidates and preparation for the incorporation of the selected person

Where to find us

IrsiCaixa

Germans Trias i Pujol Hospital | 2nd floor, Maternity building.

Ctra. del Canyet, s/n. 08916 Badalona, Barcelona

(+34) 93 465 63 74