Medical Advisor Medical Monitor information
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$21.49 is the 25th percentile. Wages below this are outliers.
$15.14 - $22.71
30% of jobs
$22.71 - $30.27
2% of jobs
$30.27 - $37.83
0% of jobs
$37.83 - $45.39
4% of jobs
$45.39 - $52.95
13% of jobs
The median wage is $53.45 / hr.
$52.95 - $60.51
16% of jobs
$60.51 - $68.07
3% of jobs
$68.07 - $75.63
6% of jobs
$76.01 is the 75th percentile. Wages above this are outliers.
$75.63 - $83.19
11% of jobs
$83.19 - $90.76
13% of jobs
$90.76 - $98.32
2% of jobs
How much do medical advisor medical monitor jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for medical advisor medical monitor in the United States is $53.85, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $78.37 per hour, depending on experience, location, and employer.
Medical Advisor Medical Monitors are healthcare professionals who oversee the safety and scientific integrity of clinical trials. They are responsible for monitoring patient safety, evaluating adverse events, and ensuring that studies comply with regulatory requirements and ethical standards. Their role bridges clinical practice and research, providing medical expertise to study teams and helping to interpret clinical data. They also act as a key point of contact between sponsors, investigators, and regulatory authorities throughout the trial process.
A Medical Advisor Medical Monitor works closely with clinical research teams by providing medical oversight throughout the course of a clinical trial. They review safety data, address medical queries from investigators, and ensure the study protocol is adhered to from a medical perspective. Regular meetings with data management, regulatory, and pharmacovigilance colleagues are common to discuss patient safety, protocol deviations, and emerging data. This role requires excellent communication skills as they bridge clinical, regulatory, and operational teams to ensure participant safety and trial integrity.
To thrive as a Medical Advisor Medical Monitor, you need a strong medical background (such as an MD or PharmD), clinical research experience, and deep knowledge of therapeutic areas relevant to the trials. Familiarity with clinical trial management systems (CTMS), medical safety databases, and regulatory guidelines like GCP and ICH is essential, and certifications in clinical research can be advantageous. Excellent communication, critical thinking, and teamwork skills help you interpret data, provide medical guidance, and collaborate with cross-functional teams. These capabilities are vital to ensure patient safety, regulatory compliance, and the successful execution of clinical trials.
What are popular job titles related to Medical Advisor Medical Monitor jobs?
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