Clinical Trials Coordinator For The Usic

buscojobs España; Las Palmas de Gran Canaria; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading healthcare organization in Spain seeks a Clinical Trials Coordinator to manage and support various research trials. This full-time role involves coordinating research teams, managing clinical trial processes, and handling administrative tasks related to clinical studies. The ideal candidate will possess a Bachelor's degree and in-depth knowledge of clinical protocols, alongside strong coordination and monitoring abilities.

Formación

• In-depth knowledge of study protocols.
• Experience in clinical trial management.
• Effective communication and coordination skills.

Responsabilidades

• Coordinate clinical trials and research teams.
• Manage patient scheduling and data entry.
• Prepare and submit necessary documentation for clinical studies.

Conocimientos

Coordination

Monitoring and audits

Biological sample management

Administrative tasks

Educación

Bachelor's degree

Descripción del empleo

Research Field : Medical sciences

Researcher Profile : Other

Profession : Positions Bachelor

Country : Spain

Type of Contract : Temporary

Job Status : Full-time

Funding : Not funded by a EU programme

Research Infrastructure : No

Offer Description

The selected person will join the USIC to manage and support various trials and will carry out the following tasks :

• Coordinator in clinical trials of laboratories and studies promoted by researchers from the HUAV and HUSM :
• Coordinate the research team of clinical trials developed in the Clinical Trials Unit.
• 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 agendas and preparing visits.
• Data entry into the CRF.
• Biological Sample Management : Sample processing and management of sample collection / shipment to external laboratories.
• Other related tasks as needed.
• Administrative tasks in the management of clinical studies :
• Submission and processing of documentation to CEIm and AEMPS.
• Processing of insurance documents or actions related to clinical trials.
• Review and update of rates.
• Preparation of budgets and invoicing proposals.

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