hirly

Fortrea

CRA II - FSP, Romania

Bucharest · Remote Romania

hirly Pro

Get in front of the people hiring at Fortrea

  • Reach the hiring manager at Fortrea on LinkedIn, from your own account
  • hirly applies to this job for you, with unlimited applications
  • A resume and cover letter written for this job, unlimited
  • The hiring manager and recruiter at Fortrea, with contact details
Get Pro for this job →

$49 a month · ₹1,999 for 30 days in India · cancel any time

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Fortrea first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 3M live jobs from 220,000+ employers in 200+ countries.

Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude or ChatGPT and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Mid level
Country
RO
Work mode
On-site / unstated
First seen by hirly
3 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

This may be time for you to join our innovative FSP team as a Clinical Research Associate (CRA) in Romania and be at the forefront of groundbreaking medical advancements in a variety of indications (Oncology, Neurology, Gene Therapy...).

Key Responsibilities:

  • Monitor Clinical Trials - conduct site visits to ensure compliance with protocols, regulatory requirements and Good Clinical Practice (GCP)
  • Site Management - Serve as the primary point of contact for investigational sites, ensuring smooth study operations.
  • Source Document Verification (SDV) - Review and verify accuracy of clinical data collected from study sites.
  • Investigator Training and Support - Provide ongoing training to site staff on study protocols and regulatory requirements
  • Reporting and Documentation -Prepare monitoring reports, maintain study records, and contribute to overall trial documentation.

​​ Qualifications:

  • Life Sciences University degree or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). (Fortrea may consider relevant and equivalent experience in lieu of educational requirements)
  • Thorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements .
  • Thorough knowledge of monitoring procedures and basic understanding of the clinical trial process.
  • Fluency in Romanian and in English , both written and verbal.

What We Offer:

  • Flexible work arrangements (hybrid /remote options)
  • Career growth environment in a supportive environment
  • Dedicated Line Manager
  • Works directly with a leading sponsor on innovative studies
  • Attractive salary and Fortrea benefits

If you are passionate about clinical research, thrive in a collaborative environment, and seek exciting career growth, we want to hear from you!

#LI-Remote #LI-Hybrid

Learn more about our EEO & Accommodations request here .

Original posting on Fortrea's site ↗

Listed on hirly, a job board. hirly is not the employer: Fortrea is hiring for this role.

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job