Fecha de publicación: 24 jul 2026

Ciudad: Madrid

País/región: ES

Tipo de contrato: Fijo

ID de solicitud de trabajo: 12387

CRA

CRA

POSITION TITLE: CLINICAL RESEARCH ASSOCIATE (CRA)

REPORTS TO: Project Manager

LOCATION: MADRID (SPAIN)

MISSION: Ensure that clinical trials are conducted, documented, and reported in full compliance with the study protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements. The purpose is to protect the rights, safety, and well-being of study participants while ensuring the quality, integrity, and reliability of the data collected.

REQUIREMENTS FOR THE POSITION :
Experience

3-4 years as CRA

At least 2 years Oncology experience

Extensive experience in monitoring oncologic patients across multiple clinical trials

Experience of monitoring of phase 2-3 and pivotal studies, Phase 1b is an add on

Able to manage complex design, including SIVs,



monitoring during recruitment phase

Demonstrate by management of a substantial number of sites / subjects.

Skills:
Communication: strong interpersonal and negotiation skills with investigators and site staff

Problem-solving: Ability to identify and resolve protocol deviations or compliance issues

Organization: Strong attention to detail and ability to manage multiple sites/projects proactively

Time management skills: ability to work independently and manage multiple tasks effectively

Agility: demonstrate ability to adapt to new tools, processes and technologies in clinical researc

IInterest and capacity to learn new ways of working and increase scope of responsibilities to grow in the role

Languages

Spanish: business level

English: business slevel

Others:
Driven licence

CRA

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