Research Support Technician (2024.41)

16 Apr 2024
Job Information

Organisation/Company

IDIVAL

Department

Human Resources Department

Research Field

Pharmacological sciences » Clinical pharmacology

Researcher Profile

Recognised Researcher (R2)

Country

Spain

Application Deadline

25 Apr 2024 - 23:59 (Europe/Brussels)

Type of Contract

Permanent

Job Status

Full-time

Hours Per Week

35h/ week

Offer Starting Date

16 Apr 2024

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

Skills/Qualifications

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.

Specific Requirements

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
Benefits

ANNUAL GROSS SALARY

42.992,38 € without prejudice to the basic update established in state legislation for 2024.

Eligibility criteria

• 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

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

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

Where to apply

Website

https://www.idival.org/es/empleo

Contact

State/Province

Cantabria

City

Santander

Website

https://www.idival.org

Street

C/ Cardenal Herrera Oria, s/n

Postal Code

39011

STATUS: EXPIRED