Senior Clinical Research Associate

🔥 0 minutes ago

🇸🇰 Slovakia – 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

• Work on the frontline of communication with project stakeholders • Ensure timelines, targets and standards of clinical research projects across therapeutic indications • Build and maintain relationships with clinical sites and investigators • Focus on subjects’ rights, safety and well-being and quality of data compliance • Conduct and report all types of onsite monitoring visits • Drive the study startup phase, if applicable • Perform CRF reviews, source document verification and query resolution • Manage site communication and activities • Supervise study activities, timelines, and schedules for each site • Act as a point of contact for in-house support services and vendors • Support quality control, including compliance monitoring and report review • Participate in feasibility research • Support the regulatory team in preparing documents for study submissions and regulatory approval

🎯 Requirements

• BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience • Independent on-site monitoring experience in Slovakia, ideally on multiple projects at a time • Demonstrable experience in all types of monitoring visits in Phase II and/or III • Strong written and verbal communication skills • Fluency in Slovak and English • Experience supporting Oncology studies is beneficial, but not essential • Intermediate to Advanced knowledge of MS Office • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills are essential • Full and clean driver's license • Ability to travel

🏖️ Benefits

• Employees can work remotely • Professional development and career investment • Recruitment guidance and support throughout the process