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:
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Obtenga más información sobre las tareas generales relacionadas con esta posibilidad a continuación, así como sobre las habilidades requeridas.
- 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/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? xhfqzwm
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.