Job Information
- Organisation/Company
- IDIVAL
- Department
- Human Resources Department
- Research Field
- Pharmacological sciences » Clinical pharmacology
- Researcher Profile
- Recognised Researcher (R2)
- Country
- Spain
- Application Deadline
- Type of Contract
- Permanent
- Job Status
- Full-time
- Hours Per Week
- 35h/ week
- Offer Starting Date
- Is the job funded through the EU Research Framework Programme?
- Not funded by an EU programme
- Reference Number
- 2020.279
- Is the Job related to staff position within a Research Infrastructure?
- No
Offer Description
ACADEMIC DEGREE
Specialist in Clinical Pharmacology (Justification must be provided with the application).
FUNCTIONS
Support the development of clinical trials throughout their development with the following tasks:
o Coordination and comprehensive planning of patients' agendas for their participation in clinical trials.
o Attention to trial subjects in the Valdecilla Clinical Trials Unit, and specifically assistance in emergency and urgent situations.
o Monitoring of the quality system
o Interlocution with the investigators and monitors for the development of clinical trials.
o Supervision of the tasks of drug administration, test performance, sample shipment, etc. o Supervision of the information systems of the clinical trials.
o Supervision of the information systems used in the clinical trials.
Requirements
- Research Field
- Pharmacological sciences » Clinical pharmacology
- Education Level
- PhD or equivalent
FURTHER
Experience as clinical trial coordinator
Experience as an investigator-subinvestigator in clinical trials.
OTHERS
Training in the field of clinical trials (good clinical practice in clinical research, clinical trial monitoring, IATA, etc.).
Training in Emergency Medicine
Research (publications and communications to conferences) in the field of clinical pharmacology.
ACADEMIC DEGREE
Specialist in Clinical Pharmacology (Justification must be provided with the application).
OTHERS REQUIREMENTS
English level B2 (Justification must be provided with the application).
- Languages
- ENGLISH
- Level
- Good
Additional Information
ANNUAL GROSS SALARY
42.992,38 € without prejudice to the basic update established in state legislation for 2024.
- Experience as clinical trial coordinator MAXIMUM 20
- Experience as an investigator-subinvestigator 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
- Research (publications and communications to conferences) in the field of clinical pharmacology. MAXIMUM 10
SELECTION PROCESS STAGES
1. Admission of applications.
2. Competition phase.
3. Interview pase: maximum number of candidates to be interviewed: 3. Minimum score for this
phase: 40.
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: Mª Blanca Sánchez Santiago, head of the Valdecilla Clinical Trials Unit and Principal Investigator of the Project.
Member: Francisco Galo Peralta, IDIVAL Management Director.
Member and secretary: Maria José Marín Vidalled, Coordinator of IDIVAL's Technological Services.
- Website for additional job details
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
Where to apply
- Website
Contact
- State/Province
- Cantabria
- City
- Santander
- Website
- Street
- C/ Cardenal Herrera Oria, s/n
- Postal Code
- 39011