
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.
🔥 21 hours ago
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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.
• Serve in part as a Strategic Site Relationship Manager • Establish and maintain strong relationships with clinical investigators, key opinion leaders, sites, and site staff • Provide insights and feedback to internal teams and sponsors • Conduct targeted conversations regarding operational challenges, including patient recruitment and retention • Hold clinical and scientific discussions to ensure quality study endpoints • Support optimal site selection and help sites understand protocols and enroll appropriate trial participants • Support and guide project teams with site identification and selection • Support project teams regarding site performance issues • Proactively manage study site issues to maintain study timelines and quality • Initiate, recommend, and communicate corrective actions as needed
• A doctoral degree is required, or alternatively, a bachelor's/master's degree accompanied by experience as an advanced practice provider, such as a Physician’s Assistant, Nurse Practitioner, or another licensed healthcare provider • Minimum of 7 years’ experience in clinical research in academia, Pharma, Biotech or CRO, including background in operational aspects of clinical research • At least 3 years as CTL or Medical Science Liaison preferred • Minimum of 3 years’ experience in the therapeutic area/indication assigned • Demonstrated experience working directly with clinical sites and investigators • Demonstrated customer service and relationship building skills with clinical sites (on site and remote) • Excellent networking skills • Excellent written and verbal communication skills • Excellent negotiation, influencing and problem-solving skills • Self-motivated with proactive issue monitoring and management, including risk assessment and contingency planning • Critical thinking and operational expertise and efficiency • Ability to work independently
• Competitive benefits package depending on location • Transparent compensation and pay equity
Apply Now🕒 August 26
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