Research technician (t3), level 2 – 16 t, study coordinator (España)

Research technician (t3), level 2 – 16 t, study coordinator (España)

08 nov
|
Incliva Biomedical Research Institute
|
España

08 nov

Incliva Biomedical Research Institute

España

Organisation/Company INCLIVA Biomedical Research Institute Research Field Medical sciences » Health sciences Researcher Profile Other Profession Positions Bachelor Positions Application Deadline 18 Nov 2026 - 23:59 (Europe/Madrid) Country Spain Type of Contract Permanent Job Status Full-time Hours Per Week 37,5 Offer Starting Date 1 Dec 2026 Is the job funded through the EU Research Framework Programme? Horizon 2020 Reference Number 105/2026 Is the Job related to staff position within a Research Infrastructure? No

Offer Description

The INCLIVA Foundation is a Health Research Institute accredited by the Carlos III Health Institute and as such an Agent of the National Science and Technology System. It is part of the public sector of the Generalitat, has legal personality of a private nature, and is governed by the private legal system and its specific legislation, without prejudice to the rules of public law that are applicable to it.

Accordingly, applications are invited for the position of Research Technician (T3), Level 2 – 16 T (Study Coordinator) to work on the project “PRIME-CKD (Personalized Drug Response: Implementation and Evaluation in Chronic Kidney Disease), Activity: HORIZON-HLTH-2022-TOOL-11-01 , and to support clinical trials conducted by the Nephrology Department, Renal Disease Research Group, Cardiovascular Area, under the supervision of Dr José Luis Górriz .

Functions to perform:

- Responsible for planning, organising, managing and coordinating activities. Carrying out administrative, management and/or technical tasks; supervising and supporting other team members; leading activities and ensuring their proper implementation.
- Managing documentation and maintaining the database.
- Preparing, curating and filtering data obtained from samples. Ensuring that the data generated from the samples are accurate, consistent,



meet the required quality control criteria and are ready to be uploaded to the project's genomic data management platform.
- Selecting and integrating the data sources that will support the system.
- Attending project research team meetings.

1. EDUCATIONAL QUALIFICATIONS (10–75 points)

1.1. Master's degree in Clinical Trials (CT), provided it is an officially recognised qualification (at least 60 ECTS credits or equivalent in hours). In the case of university-specific qualifications and/or non-official Master's degrees in Clinical Trials (at least 60 ECTS credits or equivalent in hours), 7.5 points will be awarded per qualification. Maximum: 10 points.

2. LANGUAGES (5–15 points)

2.1. Knowledge of English:

- B1 level: 2 points.
- B2 level: 3 points.
- C1 level: 4 points.
- C2 level: 5 points.

3. PROFESSIONAL EXPERIENCE AND SKILLS RELEVANT TO THE POSITION (0–75 points)

3.1. Proven professional experience in clinical trial coordination and nursing activities in the field of nephrology: 10 points per year of experience, up to a maximum of 60 points. Periods of less than one year will be calculated on a pro rata basis for each full month worked.

3.2. Authorship of research outputs: scientific publications (5 points per publication, up to a maximum of 15 points).

Degree of functional diversity equal to or greater than 33%. 10 points

Being a victim of gender violence. 10 points

Personal interview. 10 points

Specific Requirements

- Bachelor's Degree or Diploma in Nursing,



in accordance with the applicable curriculum requirements (MECES Level 2 / EQF Level 6).
- Possess physical and mental capacities and aptitudes that are necessary for the performance of the corresponding functions or tasks, which will be accredited by the applicant by means of a responsible declaration, at the time of registration of the call.
- Have Spanish nationality or work permit, or some other nationality that allows access to public sector employment
- To be at least 16 years of age and not to exceed, where appropriate, the maximum age of compulsory retirement or any other age that may be established by law.
- Not incur in any cause of incompatibility that prevents the performance of functions under the general regime with an entity belonging to the public sector,
- Not to be disqualified by a final judgment from exercising functions similar to those of the category or professional group to which access is sought.
- In the event of having previously provided services in the INCLIVA Foundation, not having been disiplinarily dismissed in a disciplinary manner by the Foundation.
- In the case of having previously provided services in the INCLIVA Foundation in the position offered, having passed the probationary period of the sam

Languages ENGLISH Level Good

Research Field Medical sciences » Health sciences

Additional Information

Selection process

The notifications and resolution of the selection process will be published on the employment portal of the INCLIVA website.

Additional comments

Applications must be registered through the EMPLOYMENT portal enabled on the INCLIVA website, attaching the documentation:

- Self-assessment form.
- ID.
- Resume
- Qualifications required.
- Documentation that accredits the necessary requirements of the call.

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📌 Research technician (t3), level 2 – 16 t, study coordinator (España)
🏢 Incliva Biomedical Research Institute
📍 España

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