Medical Director – Contract

🕒 September 30

🐊 Florida – Remote

🐊 Florida – Remote

⏱ Part Time

🔴 Lead

👨‍⚕️ Medical Director

👻 Ghost score 24%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Open for 46 days.
• Jobs at this company usually fill in 21 days.
• No salary listed.

Apply Now

Check your resume score

Customize resume + cover letter

Find Similar Remote Jobs

☆ Save☑️ Mark as applied❌ Hide

Report problem

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 support and related meetings • 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 based on clinical and medical team input • Develop strategies for FDA submissions • Develop protocols • Prepare drafts of appropriate study plans • Assist medical monitoring in clinical trial management

🎯 Requirements

• MD or PhD in Gastroenterology & Hepatology 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 Gastroenterology and Hepatology • Strong communication • Medical writing • Ability to work independently • Excel • CTMS • Willingness to work in shifts as and when needed

🏖️ Benefits

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

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume