Senior Clinical Trial Manager – Oncology

🔥 7 minutes ago

🇪🇺 Europe – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Lead and coordinate clinical site management activities from study startup through database lock and study closeout • Partner with project management to develop monitoring strategies, establish site management targets, and ensure delivery against project goals • Provide leadership, guidance, and oversight to CRAs and site management team members across assigned studies and regions • Serve as the primary site management representative for sponsors, study teams, investigator meetings, audits, inspections, and key project discussions • Drive quality and compliance by overseeing monitoring activities, reviewing protocol deviations, ensuring adherence to Clinical Monitoring Plans, and maintaining inspection readiness • Monitor study metrics, recruitment performance, resource allocation, and operational trends to identify risks and implement solutions • Support patient recruitment efforts by tracking enrollment progress and guiding site-specific recruitment strategies • Ensure Trial Master File compliance and oversee timely completion and quality review of site management documentation • Identify, escalate, and mitigate operational and monitoring risks while supporting issue resolution and continuous improvement • Collaborate with project management, sponsors, CRAs, and cross-functional teams across multiple time zones

🎯 Requirements

• Four-year college curriculum or equivalent with a major concentration in biological, physical or health studies and a minimum experience of 4 years as a Senior Clinical Research Associate (or equivalent), OR • Two-year college curriculum or equivalent education/training and a minimum experience of 6 years as a Senior Clinical Research Associate, AND a minimum 2 years relevant experience as a CTM/LCRA (or equivalent) including overseeing a CTM team • Nursing degree or equivalent life science degree preferred • Experience working with Oncology studies is required • Experience leading or coordinating clinical monitoring and site management activities within clinical trials • Strong understanding of clinical research principles, site management processes, and monitoring best practices • Knowledge of FDA and/or EU regulations, ICH Guidelines, local regulatory requirements, and clinical trial SOPs • Experience reviewing study metrics, managing operational risks, supporting recruitment activities, and maintaining high-quality study documentation • Proficiency with Microsoft Office and clinical systems including EDC, CTMS, IxRS/IVRS, and eCRF platforms • Ability to lead and motivate remote teams, influence stakeholders, solve complex problems, and manage multiple priorities • Proficiency in English, with excellent written, verbal, presentation, and interpersonal communication skills

🏖️ Benefits

• Equal employment opportunities • Diverse and inclusive work environment • Hands-on, accessible leaders • Cohesive and supportive teams • Professional growth and success enablement • Remote work arrangement • Travel on an as-needed basis