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 general 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: United States
* Visa & relocation support included
* Long-term assignment (2–3 years)
What are we looking for?
* Minimum 4 years of experience as a CRA in clinical trial monitoring
* Strong experience performing:
o Site Selection Visits (SSV)
o Site Initiation Visits (SIV)
o Routine Monitoring Visits (RMV)
o 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
As a CRA, you will play a critical role in the successful execution of international clinical trials across multiple sites in the United States. 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
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