Senior Clinical Trial Manager – Oncology

🕒 Yesterday

🇵🇱 Poland – 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

• Provide leadership and direction to clinical site management team members from study start through closure • Oversee regional CTMs and coordinate efforts across the CTM team • Represent Site Management issues at Sponsor, Investigator, and bid defense meetings • Act as the main point of contact for study activities • Contribute to the overall project plan and formulate global monitoring strategies across assigned regions • Assign sites on behalf of the sponsor • Assume a dual PM/CTM role when needed • Develop, maintain, and ensure compliance with Clinical Monitoring Plans, including budgets, study tools, and site visit reports • Review protocol deviations, out-of-scope items, and action items • Train and manage the CRA team on clinical aspects of the study • Participate in recruitment strategy development and implementation • Forecast site visits with the CRA team to ensure staffing needs and address backlogs • Mentor CTMs when needed • Perform co-monitoring visits • Review and finalize trip reports according to WCT SOPs • Support study teams during healthcare authority inspections or sponsor audits

🎯 Requirements

• Excellent interpersonal, oral, and written communication skills in English and in local language • Ability to lead and motivate a team remotely • Initiative and problem-solving skills • Strong customer focus and professional interaction with sponsors • Proficiency in Microsoft Office, CTMS, and EDC systems • Four-year college curriculum or equivalent with a major concentration in biological, physical, or health studies and minimum 4 years as a Senior Clinical Research Associate or equivalent • OR two-year college curriculum or equivalent education/training and minimum 6 years as a Senior Clinical Research Associate • Minimum 2 years of relevant experience as a CTM/LCRA or equivalent, including overseeing a CTM team • Experience working with Oncology studies is required • Willingness to travel

🏖️ Benefits

• Diverse and inclusive work environment • Supportive, team-oriented atmosphere • Hands-on, accessible leadership • Equal employment opportunities • Employee experiences where everyone is respected and has access to equal opportunity