Organisation/Company: Institut d'Investigacio Biomedica de Bellvitge (IDIBELL)
Department: RRHH
Research Field: Biological sciences » Biology
Researcher Profile: First Stage Researcher (R1)
Positions: Bachelor Positions
Country: Spain
Application Deadline: 28 Nov 2024 - 23:59 (Europe/Madrid)
Type of Contract: Temporary
Job Status: Full-time
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 Study Coordinator – USRC (Non-clinical staff) - Replacement position
Ref.24-150_SS_MG
About the research group
The clinical research support unit (Unitat de Suport a la Recerca Clínica-USRC) was established in 2018 as part of the Clinical Research Department at IDIBELL to provide support to the researchers at Hospital Univeritari de Bellvitge (HUB) for conducting clinical trials & research studies.
Currently the unit is engaging more than 80 studies of different therapeutic areas through scientifico-tecnic, administrative and execution support.
About the role
We are looking for a full-time study coordinator to contribute to the development and implementation of different research projects and to work in a multidisciplinary team being responsible for the day-to-day of clinical studies carried out at Hospital Universitari de Bellvitge.
The research staff will work and interact with a multidisciplinary team including physicians, research coordinators, and pharmacists.
Main tasks and responsibilities:
Monitor the participants' medical condition and schedule and conduct research protocol follow-ups.
Provide information to potential participants in clinical research studies.
Selection, inclusion and follow-up of patients in clinical research studies.
Collect blood and other biological samples from patients participating in clinical research studies following all research procedures within approved study protocols.
Handle biological samples: centrifuge, freeze, ship to central laboratories, etc.
Carefully monitor the patient during the administration of the investigational drug.
Participate in the meetings and activities of the Research Group.
Coordinate clinical research studies in different therapeutic areas.
Responsible for the researcher's archive.
Support Investigators to carry out study procedures.
Provide guidance on the organization of all clinical studies.
Review and update regulatory submission documents as required by the protocol.
Coordinate study visits and medical tests.
Maintain the Investigator site file.
Data entry in the eCRF from different source documents.
Collect data as required by the protocol. Assure timely completion of Case Report Forms.
eCRF data entry and queries resolution.
Job requirements
Professional experience:
At least one year in a similar position.
Education and training:
Degree in Life Sciences.
Bachelor's Degree in nursing.
Technical & soft skills:
Knowledge of medical terminology.
Problem solving.
Motivation, initiative, and ability to learn.
Good organizational skills with attention to detail.
Collaborative and teamwork skills.
Good IT competence: MS Windows and Office applications.
Good communication and teamwork skills.
High motivation and initiative.
Results orientation.
Languages:
Good command of the English language.
Catalan and Spanish spoken and written.
We will value, but not required:
Knowledge of the ethical and legal norms that regulate clinical research.
Flexibility and adaptability to different therapeutic areas.
Knowledge/experience in the national health system.
Command of eCRF and Clinical trial management platforms.
What do we offer:
No. of positions: 1
Estimated start date: as soon as possible.
Contract duration: Temporary contract to cover sick leave.
Estimated annual gross salary: € 28.000.
You will be part of a multicultural team. We have a fun loving and friendly international work environment.
Flexible working schedule: We know you have a life outside of work and we will work with you to make sure it's kept that way.
26 working days of holiday: per year.
System of accumulated hours: for employees, from 88 to 104 hours depending on the year (11 to 13 working days), to attend to personal matters.
Paid leave package.
Benefits of constant training are offered.
We offer and promote diverse and inclusive conditions. Applicants are made free from any discrimination. Specifically, IDIBELL works to improve gender equality in all areas with the aim of achieving gender balance, but maintaining the most scrupulous respect to any choice at the level of gender identity. Please express yourself freely, safely and non-binarily, if that's the case.
Deadline: Please submit your application by 28/11/2024.
#J-18808-Ljbffr