Clinical Trial Manager – Real World Evidence

🔥 0 minutes ago

🌐 Bulgaria, Poland, +2 more countries – Remote

🇧🇬 Bulgaria – Remote 🇵🇱 Poland – Remote 🇬🇪 Georgia – Remote 🇿🇦 South Africa – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Provide operational oversight of milestones and activities for assigned projects • Manage site management and monitoring activities, including remote site management by SMAs and onsite monitoring by CRAs • Oversee site activation, site communication, visit planning, document collection and maintenance, regulatory approvals, and site close-out • Document clinical activities within a Clinical Trial Management System (CTMS) • Develop site monitoring and management plans • Develop and conduct training for the clinical team • Review trip reports and proactively identify risks and mitigation strategies • Review metrics and dashboards supporting clinical operations oversight • Lead data review and query management activities as needed • Collaborate with the RWS Project Manager, Finance, and Data Management to deliver within scope, timeline, and budget • Provide sponsors with metrics and key study updates • Plan and manage clinical operations aspects of trials/studies • Collaborate with global cross-functional teams on protocols and procedures • Build and manage relationships with investigators and stakeholders • Ensure compliance with applicable regulations and ethical guidelines • Make decisions regarding trial design, vendor selection, and risk management • Lead the clinical team to deliver studies according to sponsor expectations

🎯 Requirements

• University degree in medicine, science, or equivalent combination of education & experience • At least 2 years’ experience in the similar role / in CRO or Pharma company • In depth RWE Clinical Trial Management exposure • Demonstrated ability to drive the clinical deliverables of a study • Worked across different clinical studies in various therapeutic areas in Phases III and/or IV • Prior experience with risk-based monitoring (RBM) oversight is desirable • Willingness to travel as required (approximately 15%) • Ability to work on multiple project/clients simultaneously on assigned FTE • Demonstrated strong time management skills • Experience in non-interventional studies is a plus but not required • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways