Medical Director – Contract

🕒 July 16

🐊 Florida – Remote

🐊 Florida – Remote

⏱ Part Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 44%

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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Sitero

WebsiteLinkedInAll Job Openings

201 - 500 employees

🏥 Healthcare

💼 Consulting

⚕️ Healthcare Insurance

Healthcare • Consulting • Healthcare Insurance

Sitero is a next-generation clinical trial solutions provider that accelerates clinical trials, ensures compliance and safety, and enables innovation through advanced technology and world-class services. They offer a wide range of clinical services, including site support and activation, data management, biostatistics, and drug safety. Sitero specializes in eClinical technology, providing end-to-end, technology-enabled services such as electronic data capture, randomization and trial supply management, clinical trial management systems, electronic consent solutions, and payment systems. Their services also include IRB ethical review, biosafety consulting, and pharmacovigilance agreements, ensuring comprehensive support for clinical research organizations.

📋 Description

• Provide strategic input into current and potential clinical projects • Support site investigators • Manage medical monitoring and all medical aspects of clinical trials • Provide strategic input for proposal writing and bid-defense meetings • Support data review and medical writing for protocols and study-specific reports, including regulatory annual reports and clinical study reports • Support FDA interactions, including IND and IDE meetings and submissions • Review and address site and CRA queries regarding inclusion/exclusion criteria • Prepare listings of protocol deviations and adverse events for regular meetings • Perform initial review for coding and reconcile coding with clinical and medical team inputs • Develop strategies for FDA submissions • Develop protocols • Prepare study plans • Assist medical monitoring in clinical-trial management

🎯 Requirements

• MD or PhD in Endocrinology or related background • Licensed MD or PhD • 2 years of experience working in clinical trials as a medical monitoring associate or equivalent relevant experience • Experience in Endocrinology • Pediatrics experience preferred • Metabolic trial experience preferred • Medical writing • Excel • CTMS • Willingness to work in shifts as and when needed • Hourly availability as project requires

🏖️ Benefits

• Variable pay • Paid time off • Healthcare benefits • Retirement benefits • Competitive salary