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A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.

You will be joining a program that takes an extensive co-monitoring approach, enabling a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on shared goals.

We are a comprehensive clinical research organization, powered by healthcare intelligence.

• Complete onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, providing instructions to site personnel, and study close-out.
• Verify the protection of study participants by confirming informed consent procedures and protocol adherence according to applicable regulations.
• Ensure the integrity of clinical data and that the study is conducted in compliance with the approved protocol, GCP, applicable regulations, and SOPs.
• Manage investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data submission.
• Verify proper management and accountability of Investigational Product (IP).
• Write and submit reports of investigational site findings and update applicable tracking systems. Escalate observed deficiencies, issues, and corrective and preventative actions as appropriate.
• Manage essential documents as required by local regulations and ICH-GCP guidelines before, during, and after a clinical study; assist with resolution of investigational site/data queries.
• Perform key risk assessments and management responsibilities throughout the project, including risk indicator and site health analysis, site process evaluation, and project escalation.
• Participate in audit preparation and follow-up activities as needed.
• Independently perform various onsite and offsite monitoring visit types.
• Gather and review information for assigned sites and identify inconsistencies. Assess risk and escalate as appropriate with limited guidance.
• Assist with non-complex adhoc, short-term assignments supporting additional studies or departmental initiatives.
• May serve as a preceptor, providing training to less experienced clinical team members.

• An undergraduate degree or international equivalent in a clinical, science, or health-related field from an accredited institution; health care professional licensure (e.g., registered nurse).
• Previous experience supporting clinical trials, including solid on-site monitoring experience.
• Willing to travel 50-80%.
• Equivalent education, training, and relevant experience may be considered. All employees must read, write, and speak fluent English and the host country language.

Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers a range of benefits focused on well-being and work-life balance for you and your family.

Visit our careers website to learn more:

At ICON, inclusion and belonging are fundamental. We are committed to providing an inclusive, accessible environment and a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need a reasonable accommodation during the application process or to perform essential job functions, please let us know through the provided form:

If you're interested but unsure if you meet all requirements, we encourage you to apply. You might be exactly what we're looking for