2026/121: 1 AC6A – Study Coordinator
Call for applications for an AC6A – Study Coordinator position at the Drug Research Centre (CIM). Application deadline: 11 September 2026 at 3:00 p.m.
About the Unit / Group
The Drug Research Centre (CIM) conducts clinical drug trials and/or clinical research in compliance with methodological, ethical and legal requirements, within the framework of international Good Clinical Practice (GCP) guidelines.
Its research activities include:
- Phase I clinical trials —with no therapeutic benefit for participants— in special populations and healthy volunteers (bioequivalence, tolerability, pharmacokinetics and pharmacodynamics, first-in-human administration).
- Phase II clinical trials.
- Collaboration with researchers from Hospital de la Santa Creu i Sant Pau in Phase II, III and IV clinical trials.
Essential requirements
- Minimum qualification required: higher education qualification —Bachelor’s degree, former university diploma or equivalent— in Health Sciences.
- Specific training in clinical trials —Master’s degree in Clinical Trial Coordination/Monitoring— or at least 2 years of previous experience in a similar position.
- Training in Good Clinical Practice and Quality standards.
- Oral and written knowledge of both official languages of Catalonia. If the selected candidate does not meet this requirement, they must demonstrate or commit to acquiring an adequate command of both official languages of Catalonia within a period not exceeding one year.
- Advanced level of English.
- Advanced knowledge of office software tools —Excel, Word, PowerPoint, etc.—.
Desirable criteria
- Professional experience in tertiary hospitals.
- Professional experience in Phase I units.
- Experience in clinical trials and data collection.
- Knowledge of Good Clinical Practice.
Duties
The selected candidate will perform, among others, the following duties:
- Coordination of clinical trials.
- Registration and enrolment procedures for participants in clinical studies.
- Management and follow-up of the scheduling of tests and visits for participants enrolled in clinical studies.
- Data management and completion of CRFs or eCRFs.
- Reporting and follow-up of adverse events.
- Assistance and support to the monitor during pre-study, initiation, monitoring and/or close-out visits.
- Preparation of the documentation required for study start-up, monitoring and audit processes.
- Management and maintenance of Investigator Site File documentation.
- Support to research staff.
We offer
- Six-month temporary contract due to production circumstances, to undertake tasks arising from a temporary and unforeseen increase in the unit’s activity.
- Annual working time of 1,627.50 hours (37.5 hours/week).
- Salary in accordance with the applicable collective agreement.
- Appointment to the PIC-CIM Research Group.
Documentation and application deadline
Interested candidates should preferably submit the documentation in PDF format by email to the Management of the Fundació Institut de Recerca de l’Hospital de la Santa Creu i Sant Pau at seleccio@recercasantpau.cat, indicating reference 2026/121:
- Application letter.
- Updated Curriculum Vitae.
- Duly signed data processing authorisation —document attached at the end of the call—.
The duly signed data processing authorisation must be attached.
The application deadline is 11 September 2026 at 3:00 p.m.