Clinical Research Associate (CRA)
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CROVELIS is currently looking for experienced Clinical Research Associates (CRAs).
This position offers the opportunity to join a integral clinical operations team supporting high-impact international studies in a fast-paced and highly collaborative environment.
Location: Madrid
What are we looking for?
Minimum 4 years of experience as a CRA in clinical trial monitoring
Strong experience performing:
- Site Selection Visits (SSV)
- Site Initiation Visits (SIV)
- Routine Monitoring Visits (RMV)
- 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/global 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 CROVELIS? xiphteb
CROVELIS is buildin

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