Logo-of-I-R-E-hiring-for-jobs-in-Romania-on-GrabJobs

Clinical Research Associate

icon building Company : I R E
icon briefcase Job Type : Full Time

Number of Applicants

 : 

000+

Click to reveal the number of candidates who applied for this job.
icon loader
Apply Now
icon loader Apply Now

Let AI Supercharge Your Job Hunt!

JobCopilot scans 500,000+ company career sites daily to find jobs for you

Never miss an opportunity Save hours by auto-filling applications forms Land more interviews with tailored applications
happy man
thunder iconActivate JobCopilot

Job Description - Clinical Research Associate

Clinical Research Associate ( CRA I & CRA II ) - Hybrid- Romania

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 experienced Clinical Research Associates to join our diverse and dynamic FSP team in Romania.
 

As a Clinical Research Associate at ICON Plc, you will play a critical role in overseeing and managing one sponsor's clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
 

What You Will Be Doing

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.

  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

  • University degree in a relevant field such as life sciences, nursing or medicine.

  • Min 8 months of experience in independent on-site monitoring of clinical trials (experience in SSVs, SIVs, IMVs , COVs)

  • Strong understanding of clinical trial processes and local regulatory requirements

  • Willingness to travel 65% of the time

  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

#LI-DS1

#LI-Hybrid

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

Original job Clinical Research Associate posted on GrabJobs ©. To flag any issues with this job please use the Report Job button on GrabJobs.
Apply Now
Share Job
Share Job

Auto-Apply to Clinical Research Associate Jobs with your AI JobCopilot

thunder icon Auto-Apply with AI

Similar Clinical Research Associate Jobs in Romania

GrabJobs is the no1 job portal in Romania, connecting you to thousands of jobs fast! Find the best jobs in Romania, apply in 1 click and get a job today!

Mobile Apps

Copyright © 2026 Grabjobs Pte.Ltd. All Rights Reserved.