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:
- 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/integral 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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