Clinical Trial Liaison

🔥 3 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $134.5k - $267.5k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

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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

• Establish and maintain relationships with key opinion leaders, sites, and site staff • Conduct targeted conversations with investigators and site staff regarding operational challenges, including patient recruitment and retention • Conduct clinical and scientific discussions to ensure quality study endpoints, protocol understanding, study feasibility, and enrolment and retention of appropriate trial participants • Convey KOL and site staff feedback to internal and external teams • Support project teams with site identification and selection based on site capabilities and anticipated protocol challenges • Support project teams regarding site performance issues and proactively manage study site issues to maintain timelines and quality • Initiate, recommend, and communicate corrective actions as needed • Serve as an alternative contact point for site issue escalations outside the CRA's scope • Assist in identifying new sites and upskilling sites for trial participation • Support business development through engagement with existing and prospective clients • Provide scientific and operational input on proposals and attend and present at bid defense meetings • Provide scientific and operational input into protocol development and review • Plan and conduct internal training for protocol understanding • Represent Worldwide Clinical Trials at relevant industry conferences and scientific meetings • Serve as a Strategic Site Relationship Manager and provide insights to internal teams and sponsors

🎯 Requirements

• Doctoral degree 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 5 years' experience in clinical research in academia, Pharma, Biotech, or CRO, including background in operational aspects of clinical research • 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 • Combination of critical thinking and operational expertise and efficiency

🏖️ Benefits

• Competitive benefits package depending on location • Transparent compensation and pay equity