L'Institut de Recerca Biomèdica de Lleida precisa incorporar un/a:

Clinical Trials Coordinator for the SCT Clinical Research Support Unit (USIC)

015-26

Status
Closed
End Date

Institut de Recerca Biomedica de Lleida is searching for a:
Clinical Trials Coordinator for the SCT Clinical Research Support Unit (USIC) at the attached document:

Professional profile of the person hired

  • Clinical Trials Coordinator

Requirements (those candidatures that do not meet this point will be excluded). These requirements must be met at the beginning of the contract.

  • Bachelor's Degree in Basic Sciences, Health or related areas
  • Catalan and Spanish level equivalent to B2
  • English level equivalent to B2

Tasks to be carried out

The selected person will join the USIC and will be responsible for managing and supporting the various clinical trials of the Nephrology Clinical Service, some of their tasks will be:

1- Perform Coordinator tasks in clinical trials:

  • Coordinate the research team of clinical trials developed in the Clinical Trials Unit
  • Have an in-depth knowledge of the study protocol and its requirements
  • Preparation and attention to monitoring and audits
  • Coordinate with the CEIC the implementation of the study. Identify, report and establish cooperation flows with the services involved
  • Scheduling patient schedules and preparing visits 
  • Data entry in the CRF
  • Biological Sample Management: Sample processing and collection/shipment management Samples in external laboratories
  • Other tasks of the role

2- Perform other administrative tasks in the management of clinical studies in case the service it requires:

  • Submission and processing of documentation in CEIm and AEMPS
  • Processing of insurance related to clinical trials
  • Rate review and update
  • Preparation of quotes and billing proposals

It will be valued

Knowledge

  • Master's Degree in Clinical Trials or Clinical Research
  • Training related to the field of Clinical Trials
  • Certificate of Good Clinical Practice in force
  • Knowledge of scientific and clinical English

Experience

  • Previous experience in a similar position within the Clinical Trials sector or in the area of clinical research
  • Experience in managing SAP software
  • Experience in the management of electronic data collection notebooks
  • Expertise in Biological Sample Processing

Competencies

  • Organizational and multitasking skills
  • Teamwork Skills
  • Creativity, empathy and enthusiasm
  • Ease of learning

Adjunts