Organisation/Company: Institut d'Investigacio Biomedica de Bellvitge (IDIBELL)
Department: RRHH
Research Field: Biological sciences » Biology
Researcher Profile: First Stage Researcher (R1)
Positions: Undergraduate Positions
Country: Spain
Application Deadline: 25 Dec 2024 - 23:59 (Europe/Madrid)
Type of Contract: Permanent
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 Data Entry - USRC REF: 24-165_SS_AG
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 scientific, technical, administrative, and execution support.
About the role
- Integration into the Clinical Research Unit and Functional Phase I Unit teams, and Investigators' teams for data entry
- Training, completion, and correction of Case Report Forms (CRFs)
- Providing support to Investigators and implementing electronic tools
- Recording trial and patient information into clinical and research applications
- Completing Serious Adverse Event (SAE) reports
- Resolving queries related to trial data
- Communicating with Sponsors and Contract Research Organizations (CROs)
- Preparation for and assistance during monitoring visits, audits, and inspections
Job requirements Professional experience
- Hands-on management of clinical trials
Education and training
- Senior Technician in Health Documentation and Administration
- Training in clinical trials
- Certified training in Good Clinical Practices
Technical & soft skills
- Proficiency in MS Office (Outlook, Word, Excel)
- Knowledge of clinical trials case report forms
- Organizational skills to plan and execute various activities, understanding their impact on the final outcome of a process
- Strong interpersonal skills, with the ability to empathize and provide assistance to others
- Capability to work effectively under pressure
Languages
- Good command of the English language
We will value, but not required
- University degree in Life Sciences
- Previous experience in data management or coordination of cancer clinical trials
- Familiarity with SAP ARGOS electronic medical record systems
What do we offer
- No.
of positions: 1
- Estimated start date: As soon as possible
- Estimated annual gross salary: 22.380,00 €
- 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.
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