Clinical Research Site Liaison II – CTO Partnerships

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🔥 0 minutes ago

🐊 Florida – Remote

🐊 Florida – Remote

⏰ Full Time

🟢 Junior

🧪 Clinical Research

👻 Ghost score 19%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Moffitt

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1961

🏭 Manufacturing

🤝 B2B

🏗️ Construction

Manufacturing • B2B • Construction

Moffitt is an industrial ventilation company with more than 60 years of experience that designs, manufactures, and installs customized ventilation systems. It offers vents, fans, evaporative cooling, heating products and provides services including free on-site evaluations, ventilation design, advanced CFD and thermal modeling, manufacturing, installation, maintenance, and turn‑key project delivery for industrial customers. Moffitt serves facilities such as data centers, glass manufacturing, metals, paper & pulp/OSB, and power generation among others.

📋 Description

• Manage day-to-day activities for external sites participating in early phase oncology clinical research trials • Provide support and oversight throughout the project life cycle • Ensure trial implementation meets Moffitt standards and complies with Moffitt processes and federal regulations • Oversee site performance, including enrollment, safety event recording and reporting, data collection, trend recognition and correction, and regulatory activities • Manage clinical research projects and influence participating stakeholders as part of progression within the career band

🎯 Requirements

• Associate’s Degree plus 5 years clinical trials experience in patient-facing coordination, data management, regulatory, or other research coordination (includes 1 year multi-site experience) • OR Bachelor’s Degree plus 3 years clinical trials experience in patient-facing coordination, data management, regulatory, or other research coordination (includes 1 year multi-site experience) • OR Master’s Degree plus 1 year multi-site clinical trials experience in patient-facing coordination, data management, regulatory, or other research coordination • Oncology experience preferred • Knowledge of clinical research regulations and processes