Project Manager, eCOA

🕒 December 1, 2025

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

👷‍♀️ Project Manager

👻 Ghost score 55%

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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Clario

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1973

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 Private Equity Round on 2019-10

Healthcare • Consulting • Logistics

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• Manage all phases of study delivery, including planning, setup, execution, monitoring, and closeout • Act as the primary point of contact for assigned studies, ensuring clear communication with clients and internal teams • Gather and document customer requirements and translate them into actionable project deliverables • Develop and maintain study documentation, monitor project milestones, and oversee study-related activities • Track project timelines, budgets, forecasts, invoicing, and scope changes to ensure successful delivery • Identify potential risks and issues, implement mitigation strategies, and escalate concerns when appropriate • Coordinate cross-functional teams throughout the project lifecycle • Present study services and project updates during client meetings and internal discussions • Support onboarding, knowledge sharing, and training of new team members • Maintain compliance with applicable processes, training requirements, quality standards, and documentation procedures

🎯 Requirements

• Bachelor’s degree or equivalent combination of education and relevant experience • 1–4 years of project management experience, preferably within pharmaceuticals, biotechnology, contract research, clinical research, or healthcare environments • Understanding of the drug development process and clinical trial lifecycle • Strong organizational, communication, stakeholder management, and problem-solving skills • Ability to manage multiple priorities while maintaining a high level of accuracy and attention to detail • Customer-focused mindset with the ability to build effective working relationships • Proficiency with Microsoft Office applications • Project Management certification or willingness to pursue professional development in project management • Valid passport and willingness to travel up to 20% as business needs require

🏖️ Benefits

• Competitive compensation • Attractive benefits focused on security, flexibility, support, and well-being • Engaging employee programs and development opportunities • Remote working • Home office allowance