CRA II

Remote from: Greece
Annual salary: Undisclosed
Salary information is not provided for this position. Check our Salary Directory to estimate the average compensation for similar roles.
Department: Healthcare & Medical
Employment type: Full Time,
Job posted: 22 May 2026
Apply before: 22 Jun 2026
Experience level: Midweight
Views / Applies: 112 / 39

About company

About ICON plc

Accelerate the development of drugs and devices that save lives and improve quality of life

Research
Dublin, Ireland, 1990

Actively Hiring

AI Summary

ICON plc is seeking a Clinical Research Associate II for a remote position based in Greece. The role involves conducting site visits, ensuring protocol compliance, and collaborating with investigators. Requires a Bachelor's in a scientific field and 2+ years of CRA experience. The job offers competitive benefits and requires 60% travel.

Job Complexity

Easy Hard

AI Insight The role demands significant travel (60%), deep regulatory knowledge, and independent work, making it challenging for mid-level professionals.

Salary Analysis

AI Insight The salary for this role is not specified, but CRA II positions in the US typically range from $55,000 to $95,000 annually. The median is around $75,000. ICON offers competitive benefits which may offset the base pay.

Key Skills

Clinical Research ICH-GCP Site Monitoring Protocol Compliance Data Integrity Patient Safety Regulatory Compliance Travel Communication Problem Solving

Cover Letter Sample

Dear Hiring Manager,

I am writing to express my interest in the CRA II position at ICON. With a Bachelor's degree in [Your Field] and over 2 years of experience as a Clinical Research Associate, I have developed a strong foundation in clinical trial management and regulatory compliance. I am proficient in conducting site qualification, initiation, and close-out visits, ensuring data integrity and patient safety.

My attention to detail and collaborative skills have enabled me to effectively resolve queries and support study teams. I am eager to contribute to ICON's mission of advancing clinical development. Thank you for considering my application.

Possible Interview Questions

Can you describe your experience with site monitoring visits and how you ensure data integrity?

I have conducted numerous site initiation, routine monitoring, and close-out visits. I ensure data integrity by reviewing source documents against case report forms, identifying discrepancies, and working with site staff to resolve queries promptly. I also verify protocol compliance and regulatory documentation.

How do you handle a situation where a site is not complying with the protocol?

I would first discuss the issue with the site coordinator to understand the root cause. Then, I would provide retraining on the protocol and GCP guidelines. If non-compliance persists, I would escalate to the project manager and consider a corrective action plan.

What strategies do you use to manage your time effectively given the travel requirements?

I prioritize tasks by urgency and impact, use a digital calendar to schedule visits and administrative work, and plan travel routes to minimize downtime. I also set aside time for documentation and follow-ups between visits.

Describe a challenging situation you faced during a clinical trial and how you resolved it.

Once, a site had significant delays in patient enrollment. I worked with the investigator to identify barriers, such as strict eligibility criteria, and suggested modifications to the recruitment strategy. We implemented a new outreach plan, which improved enrollment rates.

How do you stay updated with changes in clinical trial regulations?

I subscribe to regulatory agency updates, attend webinars, and participate in internal training. I also review ICH-GCP guidelines periodically and discuss changes with colleagues to ensure my knowledge remains current.

CRA II – Greece – Remote

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

Collaborating with investigators and site staff to facilitate smooth study conduct.

Performing data review and resolution of queries to maintain high-quality clinical data.

Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

Bachelor’s degree in a scientific or healthcare-related field.

Minimum of 2 years of experience as a Clinical Research Associate.

In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Strong organizational and communication skills, with attention to detail.

Ability to work independently and collaboratively in a fast-paced environment.
Ability to travel at least 60% of the time (international and domestic – fly and drive) and should possess a valid driver’s license.

#LI-DK2

#LI-Remote

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

Apply now >