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Clinical Trial Manager/ Clinical Research Associate

EstadoAbierta
Fecha de publicación25/06/2025
Descripción

Internal reference: 058/2025

Job Summary: IMIBIC is looking for a qualified professional to carry out scientific-technical activities, his/her main responsibilities will be the management and monitoring of the clinical trials “Randomized, Embedded, Multifactorial, Adaptive Platform trial for Community-Acquired Pneumonia (REMAP-CAP)” and “Investigation of the usability and the health economic value of the system MoodMon in monitoring of patients with a diagnosis of affective disorders”, in the Clinical Trials Unit Management Department.

Professional development opportunities: The selected candidate will receive training in relation to his/her job functions.

Investigator / Manager: Mr. José Carlos Garrido Gracia.

Department / Group: Clinical Trials Unit Management Department.  

Workplace: IMIBIC, Av. Menéndez Pidal s/n, 14004 Córdoba, España.

Number of vacancies: 1

Professional group: Assistant Technician.

Project:

  • ECRAID-Base (H2020): European Clinical Research Alliance on Infectious Diseases - This project is funded by the EU Programme Horizon 2020, Grant Agreement: 965313.
  • MoodMon (EIT Health): AI-driven patient monitoring tool for improved treatment of chronic affective disorders | This project is funded by the EU Programme EIT Health, PGA: 240037.

Contract funded by European funds: Yes

Condiciones

Salary

€1,833.33 gross/month (includes proportional extra payments)

Contract type

Scientific-technical activities contract (Art. 23 bis of Law 14/2011, of June 1st, on Science, Technology, and Innovation)

Duration

Indefinite, linked to the duration of the project or funding specified in this call.

Probationary period

6 months

Working hours

100% (40 hours/week)

Foreseen start date

July 2025

Requisitos mínimos
  1. University degree in Life and/or Health Sciences.
  2. Master's degree in Clinical Trial Monitoring.

It is mandatory to submit proof of meeting the minimum requirements and any merits subject to evaluation along with the CV (PDF format). Foreign qualifications must be validated and/or accompanied by a document certifying recognition/validation in Spain.

The email must include the call reference in the subject line along with the NIF/NIE/Passport number. Applications missing this information will not be considered.

Failure to meet these requirements will exclude the candidate from the selection process.

Se valorará
  1. Professional experience in financial management and monitoring of Clinical Trials sponsored by research managing foundations (0.5 points for every 3 months of proven experience, up to a maximum of 2 points)
  2. Experience in the development, management, and monitoring of clinical studies with medicines and/or medical devices (0.5 points for every 3 months of experience, up to a maximum of 3 points)
  3. Additional official or proprietary Master’s degree in Life and/or Health Sciences (minimum 60 ECTS; 0,5 points per official/proprietary degree, up to a maximum of 1 point)
  4. High level of spoken and written English

Language levels will be scored according to the Common European Framework of Reference for Languages (maximum 1 point):

  • English level equivalent to B1: 0,2 points
  • English level equivalent to B2: 0,5 points
  • English level equivalent to C1: 0,7 points
  • English level equivalent to C2: 1 point

Only the highest certified level will be scored.

Candidates must specify in months both the tasks and the length of professional experience. CVs that do not clearly specify the number of months of experience or relevant merits will not be considered.

Funciones
  • Management of clinical studies (clinical trials and observational studies)
  • Study medication management
  • Adverse event management
  • Support for the submission of projects to public competitive funding calls and subsequent follow-up, in close collaboration with the principal investigator and the rest of the research team
  • Monitoring of assigned studies. Preparation of reports related to the clinical trials’ monitoring (conduct monitoring visits). Availability to travel according to the frequency established in the monitoring plan of the assigned project
  • Ensure that the study is conducted in accordance with the protocol, Good Clinical Practice standards, Standard Operating Procedures, and applicable national and international regulations
  • Study quality management
Documentación a presentar

Applications must include a CV and scanned documentation proving compliance with minimum requirements and merits for evaluation.

The CV must specify the duration in months of the relevant experience or merits.

Publicidad

La presente convocatoria se publicará en los tablones de anuncios de FIBICO, así como en las páginas web siguientes:


- En la del IMIBIC (www.imibic.org)
- En la del Hospital Universitario Reina Sofía

Instrucciones de solicitud

By email to personal@imibic.org. The email must include the call reference and the NIF/NIE/Passport number in the subject line. Applications lacking this information will not be considered.

Deadline:

 

Day

Month

Year

Hour

Start Date

25

June

2025

00.00 h

End Date

05

July

2025

23.59 h

Logotipos HR Excellence in Research y Euraxess Euraxess

 

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