CRA 1

ICR United States USA

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Romania, Bucharest Until 9/25/2026 First posted July 27, 2026 Last posted July 27, 2026
Job description
Clinical Research Associate (CRA I OR CRA II) - remote - Romania

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Clinical Research Associate at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programms.

What You Will Do:

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

  • Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation

  • Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.

  • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.

  • Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required qualifications and experience:

  • University degree in medicine, science, or equivalent

  • Clinical Research Associate experience

  • Monitoring experience, experience conducting independent on-site monitoring visits and Site Initiation Visits (SIVs).

  • Experience with Site Qualification Visits (SQVs) is preferred but not mandatory.

  • Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data

  • Excellent written and verbal communication in English

  • Good social skills enabling you to deal with queries in a timely manner

  • Willingness to travel as required (approximately 60%)

#LI-NR1

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


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


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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

About this role

Summary

Conducts independent clinical trial monitoring, ensures compliance, maintains documentation, and collaborates with stakeholders.

Job title

CRA 1

Experience level

clinical research associate experience

Industry

healthcare

Location requirements

remote in Romania, Bucharest, work from home allowed

Salary

Not specified

Management role

No

Skills & keywords

Required skills

medical or science degreeclinical research experiencemonitoring experienceICH-GCP knowledgeEnglish communication

Preferred skills

site qualification visits

Specializations

clinical trial monitoringregulatory compliancemedical data review
Locations

Structured locations inferred from the posting.

Romania

Remote Country

Bucharest, Romania

Remote City