Cardio Clinical Trials Coordinator (Part-time)

Vall d’Hebron Institute of Research (VHIR) - Vall d'Hebron Institut de Recerca; Barcelona; On-site; EUR 25,000 - 38,000; Part time

Benefits offered by this job

Flexible working hours

23 days annual leave + 9 personal days

Meal vouchers

Health insurance

Transport benefits

Job summary

Vall d’Hebron Institute of Research (VHIR) invites applications for a part-time clinical trials professional in cardiovascular research within the Heart Failure Unit. The role focuses on coordinating patient visits, imaging analysis, and accurate data collection under a project-based contract.

The candidate must hold a medicine degree, be fluent in Spanish and English, and have at least 10 years in clinical trials, with familiarity in regulatory submissions (EU 536/2014), CTIS, and publications.

Qualifications

• Homologated degree in Medicine.
• Fluency in Spanish and English (professional proficiency).
• Minimum 10 years of experience in clinical trials.
• Experience in cardiovascular, lipids, renal and metabolic clinical trials.
• Strong understanding of EU Regulation 536/2014 and CTIS.
• Experience with AEMPS and CEIm regulatory and ethics submissions for clinical trials.
• Scientific publications.

Responsibilities

• Coordinate and schedule patient visits requiring on-site evaluation within the Heart Failure Unit.
• Analysis of image techniques related to heart failure.
• Collect, manage, and ensure accuracy of protocol-related clinical data.

Skills

Clinical trials experience

Regulatory submissions (AEMPS/CEIm)

CTIS / EU regulations

Publications

Fluency in English

Fluency in Spanish

Education

Medicine degree

Tools

CTIS (Clinical Trials Information System)

Job description

Vall d’Hebron Institute of Research (VHIR) invites applications for a part-time clinical trials professional in cardiovascular research within the Heart Failure Unit. The role focuses on coordinating patient visits, imaging analysis, and accurate data collection under a project-based contract.

The candidate must hold a medicine degree, be fluent in Spanish and English, and have at least 10 years in clinical trials, with familiarity in regulatory submissions (EU 536/2014), CTIS, and publications.