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.

Experience

3-4 years as CRAAt least 2 years Oncology experienceExtensive experience in monitoring oncologic patients across multiple clinical trialsExperience of monitoring of phase 2-3 and pivotal studies, Phase 1b is an add onAble to manage complex design, including SIVs, monitoring during recruitment phaseDemonstrate by management of a substantial number of sites / subjects.

Skills:





Communication: strong interpersonal and negotiation skills with investigators and site staffProblem-solving: Ability to identify and resolve protocol deviations or compliance issuesOrganization: Strong attention to detail and ability to manage multiple sites/projects proactivelyTime management skills: ability to work independently and manage multiple tasks effectivelyAgility: demonstrate ability to adapt to new tools, processes and technologies in clinical researcIInterest and capacity to learn new ways of working and increase scope of responsibilities to grow in the role

Languages

Spanish: business levelEnglish: business slevel

Others:

Driven licence

CRA

📌 CRA (Madrid)
🏢 Servier
📍 Madrid