Site Management Associate I

🕒 July 23

🇦🇷 Argentina – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 Ghost score 17%

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

• Be the key support to clinical research projects • Streamline communication, maintain systems and manage documents & information • Be the main point of contact between site personnel and CRA • Assist in pre-study testing of local site facilities • Act as the one who will ensure the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies • Ensure regulatory and ethics committee submissions • Coordinate preparation for and follow-up on audits and inspections • Manage the TMF on a site and a country level

🎯 Requirements

• College/University Degree in Life Sciences • Administrative work experience, preferably in an international settings • Prior experience working as CTA for CROs • Prior experience working in Clinical Research • Local regulations knowledge • Full working proficiency in English • Proficiency in MS Office applications • Ability to plan and work in a dynamic team environment

🏖️ Benefits

• Advance your career in clinical research • Coordinating a variety of tasks • Learning new things while growing with the company