Clinical Research Associate (CRA)
CROVELIS is currently looking for experienced Clinical Research Associates (CRAs).
This position offers the opportunity to join a global clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment.

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Location: Madrid
What are we looking for?
- Minimum 4 years of experience as a CRA in clinical trial monitoring
- Strong experience performing:

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- Site Selection Visits (SSV)

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- Site Initiation Visits (SIV)

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- Routine Monitoring Visits (RMV)

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- Close-Out Visits (COV)
- Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes
- Experience managing investigative sites independently and ensuring protocol compliance
- Ability to work in dynamic, fast-paced, and international environments
- Strong communication, organizational, and stakeholder management skills
- Previous exposure to multicountry/general clinical trials is highly valued




- Fluent English level required

Key Responsibilities
Responsibilities will include:
- Overseeing site performance and ensuring studies are conducted according to protocol, GCP, SOPs, and regulatory requirements
- Conducting site qualification, initiation, routine monitoring, and close-out visits
- Building strong relationships with investigators, coordinators, and site staff
- Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle
- Reviewing source documentation, identifying protocol deviations, and supporting issue resolution
- Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams
- Supporting site activation, enrollment, and retention strategies
- Maintaining accurate and timely study documentation and monitoring reports
- Participating in investigator meetings, trainings, and study planning activities

Why join C

📌 Clinical Research Associate (España)
🏢 Crovelis
📍 España