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 global 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:
* • 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
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
* 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?
CROVELIS is building a globally focused internal CRO designed to deliver high-quality clinical trial execution through agility, collaboration, and innovation.
This role offers a unique opportunity to combine:
✅ International relocation to the US
✅ Career growth within global clinical operations
✅ Exposure to complex and high-visibility studies
✅ Multicultural and collaborative environment
✅ Long-term international experience
If you are looking to take your CRA career to an international level and be part of a growing global organization, we would love to hear from you.