Site Management Associate – Clinical Trials

🔥 15 hours ago

🇳🇱 Netherlands – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 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

• Serve as a key point of contact for investigative sites throughout clinical research projects • Support sites in the day-to-day delivery of clinical studies • Ensure timely communication and follow-up with sites • Coordinate resolution of site-specific questions • Facilitate collaboration between sites, project teams and other stakeholders • Support site teams with project training and access to study-related and vendor systems • Track study and site activities and follow up on outstanding actions • Help keep projects on schedule • Maintain accurate study information in relevant systems • Ensure essential documentation is complete and up to date • Coordinate information and communication across internal teams and external partners • Support project meetings by drafting agendas and taking minutes • Follow up on agreed actions

🎯 Requirements

• At least 6 months of experience within clinical research • Life Sciences degree • Full professional working proficiency in Dutch and English • Good organizational and planning skills • Detail-oriented, able to multi-task and work effectively in a fast-paced environment • Good problem-solving abilities and flexibility • Team-oriented with excellent customer service and interpersonal skills • Positive attitude to tasks and projects • Proficiency in standard MS Office applications, including Word, Excel and PowerPoint

🏖️ Benefits

• Remote work • Professional development and career growth opportunities • Employer investment in employees' professional development and success