SrCRA - FSP, Romania
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 7h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 18h ago
The date the source published, not the day we noticed it (2026-10-15). Last seen at its source just now.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
Romania
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
Workday employer's own board first seen 7h ago · last seen just now
- location not stated
The listing
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 understanding of the clinical trial process.
- 3+ years of independent monitoring experience
- 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.