Clinical Research Associate (CRA) – USA Relocation Opportunity CROVELIS is currently looking for experienced Clinical Research Associates (CRAs) interested in relocating to the United States for a long-term international clinical research assignment. 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. Selected candidates will relocate to the US for an estimated period of 2–3 years, with relocation and visa support provided by the company.
Location & Travel United States
Visa & relocation support provided
Long-term assignment (2–3 years)
Qualifications 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 multi‐country/global clinical trials is highly valued
Fluent English level required
Key Responsibilities 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 p
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