11 Mar 2025
Job Information
- Organisation/Company
IDIVAL- Department
Human Resources Department- Research Field
Medical sciences » Health sciences- Researcher Profile
Recognised Researcher (R2)- Positions
Postdoc Positions- Country
Spain- Application Deadline
19 Mar 2025 - 23:59 (Europe/Brussels)- Type of Contract
Permanent- Job Status
Full-time- Hours Per Week
35- Offer Starting Date
10 Mar 2025- Is the job funded through the EU Research Framework Programme?
Not funded by a EU programme- Is the Job related to staff position within a Research Infrastructure?
No
Offer Description
ACADEMIC DEGREE
•Medical Specialist in Clinical Pharmacology/Equivalent (must be provided with the
application).
FUNCTIONS
• Supporting the development of clinical trials throughout their development with the following
tasks:
• Coordination and comprehensive planning of patients' agendas for their participation in clinical
trials.
• Care for trial subjects in the Valdecilla Clinical Trials Unit, and specifically assistance in
emergency and urgent situations.
• Monitoring of the quality system
• Interlocution with researchers and monitors for the development of clinical trials.
• Supervision of the tasks of drug administration, testing, sending of samples, etc. o Supervision
of the information systems of the clinical trials.
• Supervision of the information systems used in the clinical trials.
Where to apply
- Website
- https://www.idival.org/es/empleo
Requirements
- Research Field
- Medical sciences » Health sciences
- Education Level
- PhD or equivalent
Skills/Qualifications
VALUED MERITS /SKYLLS
EXPERIENCE
- Experience as a clinical trial coordinator
- Experience as investigator-sub-investigator in clinical trials
OTHERS
- Training in the field of clinical trials (good clinical practice in clinical research, clinical
trial monitoring, IATA, etc.).
- Master's degree in clinical research
- Research (publications and communications at conferences) in the field of clinical
pharmacology.
Specific Requirements
EXCLUSIVE REQUIREMENTS: (1)
ACADEMIC DEGREE
•Medical Specialist in Clinical Pharmacology/Equivalent (must be provided with the
application).
OTHERS REQUIREMENTS • Level B2 English (must be provided with the application).
Additional Information
Benefits
ANNUAL GROSS SALARY
43.852,23€ without prejudice to the basic
update established in state legislation for 2024.
Eligibility criteria
VALUATION OF MERITS
Experience as a clinical trial coordinator
MAXIMUM 15
Experience as investigatorsub- investigator in clinical trials
MAXIMUM 10
Training in the field of clinical trials (good clinical practice in clinical research, clinical trial
monitoring, IATA, etc.)
MAXIMUM 10
Training in Emergency Medicine
MAXIMUM 10
Master's degree in the clinical field
MAXIMUM 5
Research (publications and conference papers) in the field of clinical pharmacology.
MAXIMUM 10
Selection process
SELECTION PROCESS STAGES (2)
1. Admission of applications.
2. Competition phase.
3. Interview pase: maximum number of candidates to be interviewed: 3. Minimum score for this
phase:30
4. Report of the Tribunal.
5. Resolution.
Note: in order for candidates to be considered for recruitment and employment exchange
purposes, they must have a total score of at least 30 points.
SELECTION BOARD
• President: Blanca Sánchez Santiago, Head of the Valdecilla Clinical Trials Unit and Principal Investigator of the
Project.
• Member: Marcos López Hoyos, Scientific Director IDIVAL
• Member and secretary: Maria José Marín Vidalled, Coordinator of IDIVAL's Technological Services.
- Website for additional job details
https://www.idival.org/es/empleo
Work Location(s)
- Number of offers available
- 1
- Company/Institute
- IDIVAL
- Country
- Spain
- State/Province
- CANTABRIA
- City
- SANTANDER
- Postal Code
- 39011
- Street
- C/ Cardenal Herrera Oria, s/n
- Geofield
Contact
- State/Province
CANTABRIA- City
SANTANDER- Website
https://www.idival.org- Street
AVD/ CARDENAL HERRERA ORIA S/N- Postal Code
39011
STATUS: EXPIRED
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