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.
Por favor, lea detenidamente la siguiente descripción del puesto para asegurarse de que encaja con el perfil antes de enviar su solicitud.
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/general 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? xkdbapo
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 general organization, we would love to hear from you.