Organisation/Company: Fundación Hospital Nacional de Parapléjicos
Department: RRHH
Research Field: All
Researcher Profile: First Stage Researcher (R1)
Positions: Bachelor Positions
Country: Spain
Application Deadline: 30 Sep 2024 - 23:59 (Europe/Madrid)
Type of Contract: Other
Job Status: Full-time
Hours Per Week: 35
Offer Starting Date: 17 Sep 2024
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 To convene a selection process for the recruitment of Senior Technician (A1)/ First Stage Researcher (R1) in the Group of eosinophilic enteropathies of immunology of the digestive mucosa located in the General Hospital of Tomelloso, on a competitive basis, of the Fundación del Hospital Nacional de Parapléjicos, in charge of the research line entitled "Clinical and epidemiological aspects of eosinophilic esophagitis and inflammatory bowel diseases" with funds available in the project / grant "ADM00237" whose Principal Investigator is Dr. Alfredo J. Lucendo Villarreal.
Qualification: Degree in bio-health discipline. Minimum 2 years experience in Clinical Trials Coordination. Accreditation through certificate. Experience in the field of health care. Accreditation through certificate. Experience in dealing directly with patients. Accreditation through certificate.
Specific Requirements Experience in management and archiving of research documentation. A certificate of services and functions of the entity or group where they were provided must be presented.
Experience in electronic data collection notebooks, data entry, query resolution. Experience in the management of online platforms for clinical trials, including central laboratory, stock management, IWRS, access and management of resources from different vendors (ECG, respiratory function tests, DEXA, etc). A certificate of services and functions of the entity or group where they were provided must be presented.
Experience in management and processing of biological samples, from their collection, processing, preservation, and packaging, to their shipment. A certificate of services and functions of the entity or group where they were provided must be presented.
Knowledge in Good Clinical Practice. Accreditation through certificate or degree.
Knowledge and experience in the processing, handling and transportation of hazardous substances. Accreditation through certificate or degree.
Languages: SPANISH
Level: Excellent
Research Field: Medical sciences » Other
Years of Research Experience: 1 - 4
Additional Information The person hired will join the Eosinophilic Enteropathies Group of immunology of the digestive mucosa, led by Dr. Alfredo J. Lucendo Villarín.
Main Functions and Tasks Coordination of the following active clinical trials within the Group:
Coordination of clinical trials in a comprehensive manner.
Provide ongoing administrative support to other local team members in the development of various clinical trials, support other clinical colleagues in the progress of research.
Collaborate with site staff to ensure that clinical trials promoted by the group and by the pharmaceutical industry are conducted in accordance with the protocol and ICH GCP, as well as other applicable regulations.
Remote contact and direct face-to-face attention to patients included in clinical trials (resolution of doubts, review of records, administrative support, urgent care).
Entry of study data into electronic data notebooks and resolution of queries.
Study material management, documentation and maintenance of the investigator's file.
Coordination of the study and liaison between the different services involved.
Act as liaison with the ARCs of the different studies, providing support during the study, as well as during the initiation, monitoring and closing visits.
Document management, follow-up, archiving and electronic review.
Management of processing and shipment of biological samples.
Management of the local biological specimen bank (blood and tissue).
Manage delivery and stocking of study supplies, drug and non-drug related.
Submit documentation to CEICs, CEIm and AEMPS.
Remote management and monitoring of multicenter trials coordinated by the group.
Maintenance and management of observational study databases of the research group.
Eligibility Criteria Applicants must provide the following documents by e-mail to ****** in a single document in PDF format:
Cover letter (express mention of the reference of the offer).
Curriculum Vitae of the candidate (including mobile phone number and contact e-mail address).
Photocopy of ID card or legally accredited document.
Photocopy of the required degree or certificate of its attainment.
Documents accrediting experience (certificate of time worked or similar certificate issued by the Human Resources department of the corresponding company).
Documentation accrediting the knowledge or experience will be provided by presenting certificates issued by the company or entity in which the knowledge or experience was acquired, or, if applicable, by the entity that provided the training.
Selection Process The selection process will consist of two phases:
1st Phase: Evaluation of merits (6 points): in this phase, an evaluation of the merits and requirements established in the call for applications will be carried out by the Selection Board.
2nd Phase: Personal interview (4 points): Candidates who have obtained at least 4 points in the 1st Phase will be called for a personal interview with the Selection Board, which may be held in person or online. This interview will deal with the requirements established in the call for applications.
The Evaluation Panel will be composed of:
Chair: lead researcher /Service Manager
Member: Member of the reception group
Secretary: Human Resources of the Foundation
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