Clinical Research Associate

2 weeks ago

Romania AL Solutions Full time €40,000 - €50,000 per year

Chloe O'Shea is representing a leading global Clinical Research Organization (CRO) that delivers cutting-edge solutions to pharmaceutical, biotechnology, and healthcare partners worldwide. We are seeking a Clinical Research Associate (CRA) to join a well-established and collaborative clinical operations team in Romania.

This is an excellent opportunity for a skilled CRA to contribute to high-quality clinical research within a stable structure, benefiting from ongoing training, peer support, and long-term development in a high-performing environment.

The Role

As a CRA, you will play a pivotal role in overseeing clinical trial activities across Romania, working with experienced site teams and international sponsors. You'll ensure all trial-related responsibilities are carried out in accordance with protocols, GCP guidelines, and local regulations, while benefiting from strong internal resources and streamlined processes.

Whether you're an experienced CRA or looking to step up into more complex trials or therapeutic areas, this position offers diverse project exposure and consistent professional support.

Key Responsibilities

  • Perform all types of monitoring visits (pre-study, initiation, routine, and close-out) and generate detailed reports per internal SOPs and regulatory guidelines.
  • Develop strong working relationships with site staff to support patient recruitment, retention, and protocol compliance.
  • Ensure accurate and timely documentation, informed consent processes, drug accountability, and source data verification.
  • Oversee site adherence to GCP, local regulatory requirements, and sponsor expectations.
  • Support timely query resolution, data entry review, and tracking of essential documentation.
  • Collaborate with internal study teams to proactively identify and mitigate risks or challenges at the site level.

Requirements

  • A Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related discipline.
  • At least 1 year of independent on-site monitoring experience in Romania.
  • Strong working knowledge of ICH-GCP and local clinical trial regulations.
  • Excellent organizational skills and attention to detail.
  • Fluent in Romanian and English, both written and spoken.
  • Ability to work independently while being a collaborative team player.

What's in It for You?

  • Competitive salary with performance-related incentives.
  • A well-established and supportive team environment with structured onboarding and mentoring.
  • Access to a wide portfolio of therapeutic areas and complex global studies.
  • Long-term career progression with internal mobility and upskilling opportunities.
  • Flexible working options and balanced site visit expectations.
  • Comprehensive benefits including private medical insurance, wellness programs, and ongoing professional training.

If you're a dedicated CRA looking to grow within a global CRO that values both excellence and team support, apply now to take the next step in your clinical research career in Romania.

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