Clinical Medical Monitor

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $260k - $335k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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Praxis

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2002

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Praxis is a company dedicated to connecting patients with meaningful clinical trial opportunities. With a focus on creating customized recruitment programs, Praxis utilizes a variety of specialized tools and extensive experience across various therapeutic areas to ensure they reach the right patients worldwide. Established in 2002, the company emphasizes the importance of patient engagement and utilizes sophisticated data insights to enhance the patient journey in clinical research.

📋 Description

• Provide timely medical guidance for assigned studies, including eligibility, dosing, protocol requirements, safety events, and other study-related medical questions • Review AEs and SAEs, assessing causality, severity, expectedness, clinical significance, and potential implications for patients and the program • Respond to investigator and site medical questions while balancing patient safety, protocol requirements, and clinical judgment • Review patient-level and aggregate clinical and safety data to identify trends, inconsistencies, emerging signals, and areas requiring follow-up • Ensure medical monitoring, safety assessment, escalation, and documentation meet regulatory requirements, GCP standards, and study protocols • Work with clinical development, clinical operations, safety/pharmacovigilance, biostatistics, data management, and regulatory colleagues • Apply independent medical judgment, challenge assumptions when warranted, and determine what and when to escalate

🎯 Requirements

• MD or equivalent medical degree required; CNS or relevant therapeutic area experience preferred • Clinical trial experience with responsibility for medical monitoring, clinical safety, or related medical oversight • Strong clinical judgment and demonstrated ability to assess AEs and SAEs consistently and rigorously • Experience responding to investigator and site medical questions and making timely decisions when information is incomplete • Ability to review clinical data, recognize meaningful patterns or potential safety signals, and determine when action or additional surveillance is needed • Working knowledge of GCP, clinical trial safety reporting requirements, and documentation standards • Willingness and flexibility to travel as needed • Comfort with screen work, basic hand coordination, clear communication, and focus

🏖️ Benefits

• 99% of the premium paid for medical, dental and vision plans • Company-paid life insurance • AD&D benefits • Disability benefits • Voluntary plans to personalize coverage • Dollar-for-dollar 401(k) match up to 6% on eligible contributions • Long-term stock incentives • ESPP • Discretionary quarterly bonus • Extremely flexible wellness benefit • Generous PTO • Paid holidays • Company-wide shutdowns

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