Executive

🔥 19 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Executive

👻 Ghost score 11%

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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Atos

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

Atos is a global leader in digital transformation, providing a wide range of solutions and services across industries. The company specializes in cloud and infrastructure services, digital business platforms, technology consulting, and cybersecurity, with a focus on enhancing user experiences and supporting enterprise digital journeys. Atos is committed to sustainability and innovation, partnering with various organizations to drive digital advancements, such as its role as the official IT partner for the UEFA and the Olympic Games.

📋 Description

• Manage workflows related to clinical research regulatory activities and local submissions • Interpret reference documents and SOPs independently • Calculate visit windows, study cycles, and screening timelines • Provide meaningful feedback and constructive recommendations • Configure or build studies within CTMS and/or EMR systems such as Epic

🎯 Requirements

• 5+ years of clinical research experience • Preferably a Clinical Research Coordinator or Clinical Research Associate (CRA); Oncology experience is preferred • Experience with regulatory activities, particularly local submissions, requiring strong attention to detail and adherence to multiple protocols • Hands-on experience with Electronic Data Capture (EDC) systems and/or Clinical Trial Management Systems (CTMS) • Strong familiarity with various protocol types, including industry-sponsored studies, Investigator-Initiated Trials (IITs), NIH studies, Cooperative Group studies, and different trial phases • In depth understanding of protocol documents, including the Schedule of Events (SOE), Study Design, Synopsis/Summary, and other key sections • Excellent attention to detail and critical thinking skills • Strong knowledge of clinical research terminology, including AE, DB, OLE, LTFU, I/E Criteria, and related concepts • Ability to independently interpret reference documents and SOPs to manage workflows effectively • Good analytical and mathematical skills, including calculating visit windows, study cycles, and screening timelines • Experience providing meaningful feedback and constructive recommendations • Technical knowledge of configuring or building studies within CTMS and/or EMR systems (e.g., Epic) is highly desirable • Ability to work independently in a remote environment