Clinical Research Associate - Thessaloniki - Remote

ICON; Portland (OR); Remote; USD 70,000 - 90,000; Full time

Job summary

ICON is seeking a Clinical Research Associate to join their innovative team, focusing on the design and analysis of clinical trials. This role involves comprehensive site management and provides opportunities for training and mentorship within a global pharmaceutical client environment. Candidates should have a Bachelor's degree and experience in clinical research processes.

Benefits

Annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Qualifications

• Minimum of 1 year of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes and ICH-GCP guidelines.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Preparing and reviewing study documentation.

Skills

Organizational Skills

Communication Skills

Attention to Detail

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

Clinical Research Associate - Thessaloniki - Remote

This vacancy has now expired. Please click here to view live vacancies.

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate 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.

This role is fully sponsor dedicated and you would be working in an FSP model. Within this program, you will thrive within a fast-paced, dynamic study design. As we are fully embedded with this global pharmaceutical client, you will experience a true “one team” approach that provides limitless opportunities to develop through training, mentorship, and support from leadership.

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 1 year 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.

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 maximise 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 website to read more about the benefits of working at ICON

Impactful work. Meaningful careers. Quality rewards.

At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is to lead a global team, become a deep scientific or technical expert, work in-house with our customers, or gain experience in a variety of different ICON functions, we will support you in realizing your full potential.

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Learn more about Our Culture at ICON

If you’re seeking a rewarding and fulfilling work environment, a career at a CRO might be the perfect fit.

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