NURSE STUDY COORDINATOR/DATA ENTRY (Specialist Technician)

Offer Description

EL INSTITUTO DE INVESTIGACIONES BIOMÉDICAS DE MÁLAGA NECESITA CONTRATAR UN PROFESIONAL CON EL SIGUIENTE PERFIL: Enfermera Coordinadora de Estudios / Entrada de Datos (Técnico Especialista) .

Investigadores responsables : Elena Martín Bautista / Julián Olalla / Cristina Quero

Ubicación: Hospital Costa del Sol (Marbella)

Líneas :

Línea de implantación de principios RRI en el Hospital Costa del Sol

Línea de ensayos clínicos en VIH

Línea de ensayos clínicos en enfermedad cardiovascular

Línea de ensayos clínicos en Oncología

Funciones a desarrollar:
Apoyo en la captación de pacientes y gestión de la agenda de visitas.
Support to the main researchers in the implementation and development of the studies and collaboration in the resolution of incidents.
Administrative, management, monitoring and justification support in the area of clinical trials and management.
Data collection and ensure the quality of the data collected, adequate compliance with the electronic Data Collection Notebooks and the resolution of Queries.
Processing, registration and administration of drugs and the management and sending of samples.
Support in communication between the Project Promoter/Coordinator and the researcher (in Spanish and English).
Management of test documentation. Maintenance of the Researchers File and the rest of the study documentation.
Collaborate in the implementation of clinical studies and during the development of the trial.
Manage monitoring visits/close trials: make an appointment, prepare documents and assist the monitor.
Management of study tests for patients.
Carrying out standardized work procedures.
Support in requests for quality accreditations in the clinical trials area.
Reporting Serious Adverse Events to pharmacovigilance.
Extraction of biological samples from patients in the studies.
Coordination with the nursing team from other areas.
Establish standard operating procedures related to your work.
Maintain updated versions of the protocol and your consents.
Processing signed patient ICs, registering them and requesting tests.
Extract, process, store and send biological samples (blood, urine, biopsies, tissues) to the different central laboratories.
Take vital signs and test questionnaires from patients.
Minimum Requirements :

-Required Qualification Degree: Graduate or Diploma in Nursing

Valuable Requirements :
(Monitoring, Study Coordinator, Data Entry). Accredited by a certificate issued by a competent body or work life or Responsible Declaration. (0.5 points will be awarded/6 months worked, up to a maximum of 2.5 points).
Datatrack, Medidata, Rave, eCRFs, Rave, InForm, medPace, ClinPhone, IXRS, Oracle,. Accredited by certificate issued by a competent body, work life or Responsible Declaration. (0.5 points / 6 months worked will be awarded, up to a maximum of 1.5 points).
Accredited by certificate issued by a competent body or work life or Responsible Declaration (0.5 points will be awarded / 6 months worked, up to a maximum of 1 point).
related to clinical trials. Accredited by certificate issued by a competent body. (They will be awarded: 0.25 points per course of up to 20 hours, 0.50 for courses of more than 20 hours and 1 point per master, up to a maximum of 2 points).
Only those candidates who obtain at least 50% of the evaluable merit points will be eligible for the interview phase.

Based on the points obtained in the merit assessment, at least the three best candidates will be selected to carry out a personal interview in which communication skills, aptitude for work and skills will be assessed, with a maximum of 3 points. Candidates must obtain at least 1.5 points in the interview phase to be considered eligible.

After the resolution of the position and in the event that the selected candidate resigns from the contract, the hiring table may decide to decide in favor of the next candidate according to the published list of scores.

Contract details :
Contract modality: Employment contract for scientific-technical activities (art 23 bis of the Science and Technology Law 14/2011)
Category: Study coordinator /data entry (Technical Specialist)
Location: IBIMA/Hospital Costa del Sol (Marbella)
Gross annual remuneration: €28,000 + €2,518.98 targets (100%)
Hours: Total 100% hours (35 hours per week).
Estimated duration: 1 year extendable . The duration of the contract will be linked to the end of the project/end of the activity/end of financing.
This selection and hiring is subject to the mandatory authorization by the corresponding Ministry.

Presentation of candidatures :

Applications (including CV, accreditation/certificates of merits to be assessed and self-assessment sheet) may be submitted by e-mail: (indicate in the subject REF: LA_2023001 ) to the address

The deadline for receiving applications will end on September 23, 2023 at 3:00 p.m.

Selection process :

Tras un periodo de revisión en el que se seleccionarán los candidatos cuyo currículum mejor se adapte a los criterios establecidos, se pondrá en marcha una segunda fase consistente en una entrevista personal.

Requirements

Research Field Medical sciences » Health sciences Education Level Bachelor Degree or equivalent

Languages ENGLISH Level Good

Research Field Medical sciences » Cancer research Years of Research Experience 1 - 4

Additional Information

Work Location(s)

Number of offers available 1 Company/Institute INSTITUTO DE INVESTIGACIÓN BIOMÉDICA DE MÁLAGA Country Spain State/Province Málaga City Málaga Postal Code 29590 Street C/ Severo Ochoa 35

Where to apply E-mail

ope@ibima.eu

Contact State/Province

Málaga City

Málaga Website

Street

C/ Severo Ochoa 35 Postal Code

29590 E-Mail

rrhh@ibima.eu

STATUS: EXPIRED
EURAXESS

Fecha de publicación: 16/09/2023