Clinical Research Associate – Senior CRA

🔥 18 hours ago

🇺🇦 Ukraine – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• Prepare, conduct, and report on all types of monitoring visits, including site selection, initiation, routine monitoring, and close-out visits • Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements • Build and maintain strong relationships with investigators and site staff • Monitor patient recruitment, study timelines, and site performance • Perform source data verification, follow up on data queries, and manage site-level risks • Oversee investigational product accountability, trial supplies, and essential study documentation • Maintain Investigator Site Files (ISF) and support Trial Master File (TMF) reconciliation • Deliver study-specific training to investigators and site staff • Support regulatory submissions, audit preparation, and resolution of audit findings • Collaborate with experienced clinical research professionals across different therapeutic indications

🎯 Requirements

• MD, PharmD or MSc • 1+ year of independent on-site monitoring experience in Ukraine • Experience in all types of monitoring visits in Phase II and/or III • Experience in Oncology/Ulcerative Colitis/Antibiotics trials is a plus • Full working proficiency in English and Ukrainian • Proficiency in MS Office applications • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel

🏖️ Benefits

• Remote work in Ukraine • Opportunity to further develop skills • Opportunity to widen therapeutic area experience • Opportunity to become an expert in clinical research