Senior Clinical Trial Manager

🔥 1 minute ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $112k - $222k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

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

• Responsible for overseeing and leading the delivery of clinical study site management activities through the coordination of a team of clinical staff on particularly complex studies, such as those with significant global reach. • Uses data metrics and project planning to monitor and ensure the quality of data submitted from study sites and the timely completion of study activities, including appropriate reporting and follow-up for all safety events by site personnel. • Provide leadership and direction to clinical site management team members from study start through closure • Oversee regional Clinical Trial Managers (CTMs) and coordinate efforts across the CTM team • Represent Site Management issues at Sponsor, Investigator, and bid defense meetings and act as the main point of contact for activities throughout the study • Collaborate closely with other functions, including Business Development, Regulatory, Study Start-Up, and Project Management, to anticipate requirements and achieve study goals • Drive efforts to improve the quality of site data and deliverables and address identified needs with action plans; review data metrics to ensure data integrity and quality • Participate in the development and implementation of recruitment strategies in assigned countries and sites; lead the tracking of recruitment and revision of site-specific recruitment plans as needed to ensure enrollment remains on target

🎯 Requirements

• Four-year college curriculum or equivalent with a major concentration in biological, physical, or health studies and a minimum of four years of experience as a Senior Clinical Research Associate (or equivalent), OR • Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree preferred) and a minimum of six years of experience as a Senior Clinical Research Associate • Minimum of 2 years of relevant experience as a CTM/LCRA (or equivalent), including oversight of a CTM team • Travel required • Valid current passport required • Driver’s license required

🏖️ Benefits

• Competitive benefits package depending on location • Transparent compensation