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Clinical Medical Monitor Jobs (NOW HIRING)

Clinical Medical Monitor

$18.50 - $23.50/hr

Clinical trial experience with responsibility for medical monitoring, clinical safety, or related medical oversight. The position may be hired at the Director or Senior Director level based on the ...

Clinical Medical Monitor

OR · On-site +1

$18 - $23/hr

Clinical trial experience with responsibility for medical monitoring, clinical safety, or related medical oversight. The position may be hired at the Director or Senior Director level based on the ...

As a Medical Director, Clinical Research & Development at ICON, you will provide medical leadership and strategic direction to clinical development programs. We are looking for a board certified ...

Medical Monitor ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Medical Monitor ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

$115 - $123/hr

Director, Clinical Development III (Medical Monitor Trainer) Hourly Pay Rate: $115-123/hr (depending on candidate location/benefits preference) Length of assignment: 1 year Location: Florham Park, NJ ...

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

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Clinical Medical Monitor information

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How much do clinical medical monitor jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical medical monitor in the United States is $20.45, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $22.12 per hour, depending on experience, location, and employer.

What is the difference between Clinical Medical Monitor vs Clinical Research Associate?

AspectClinical Medical MonitorClinical Research Associate
CredentialsTypically requires medical degree or nursing license, plus clinical monitoring experienceUsually holds a bachelor's degree in life sciences or related field; may have certifications like CCRP
Work EnvironmentMonitors clinical trials at sites, reviews patient data, ensures compliance with protocolsOversees trial progress, manages site activities, and ensures data quality across multiple sites
Employer & IndustryPharmaceutical companies, CROs, biotech firms in clinical trial settingsPharmaceutical companies, CROs, biotech firms involved in clinical research

While both roles are vital in clinical trials, Clinical Medical Monitors focus on patient safety and protocol compliance at trial sites, often requiring medical credentials. Clinical Research Associates coordinate trial activities across sites, emphasizing data collection and site management. Understanding these differences helps in choosing the right career path or job search focus.

How to become a clinical medical monitor?

To become a clinical medical monitor, candidates typically need a healthcare background such as a medical degree or nursing license, along with experience in clinical research or trial management. Relevant skills include understanding regulatory requirements, Good Clinical Practice (GCP) guidelines, and familiarity with clinical trial protocols, often supported by certifications like SOCRA or ACRP. Strong communication and attention to detail are essential for overseeing trial safety and compliance.

What states have the most Clinical Medical Monitor jobs?

States with the most job openings for Clinical Medical Monitor jobs include:

What are popular job titles related to Clinical Medical Monitor jobs?

For Clinical Medical Monitor jobs, the most frequently searched job titles are:

Infographic showing various Clinical Medical Monitor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $42,540 per year, or $20.5 per hour.

Clinical Medical Monitor

Remote

Praxis Precision Medicines, Inc.
Biotechnology Research and Development • 51 - 200 employees

$18.50 - $23.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Job description

Location: This position may be performed remotely, but requires the flexibility and willingness to travel as needed.
The Opportunity
Great clinical development depends on strong medical judgment in the moments that matter: when an investigator has a question, a safety event needs assessment, or emerging data require action. At Praxis, you'll provide hands-on medical oversight for assigned clinical programs, with patient safety and study quality at the center. You'll support investigators and sites on eligibility, dosing, safety events, and other medical questions; review clinical and safety data; assess serious adverse events; and identify emerging signals or trends. You'll partner closely with clinical leads and cross-functional study teams while maintaining independent medical judgment. This is a role for someone who wants to stay close to the patients, sites, and data and make timely, thoughtful decisions that keep studies moving safely and effectively.
Primary Responsibilities
  • Medical oversight: Provide timely medical guidance for assigned studies, including eligibility, dosing, protocol requirements, safety events, and other study-related medical questions.
  • Clinical safety assessment: Review AEs and SAEs, assessing causality, severity, expectedness, clinical significance, and potential implications for patients and the program.
  • Site support: Respond promptly and consistently to investigator and site medical questions, balancing patient safety, protocol requirements, and sound clinical judgment.
  • Data surveillance: Review patient-level and aggregate clinical and safety data to identify trends, inconsistencies, emerging signals, and areas requiring follow-up.
  • Safety and regulatory compliance: Ensure medical monitoring, safety assessment, escalation, and documentation meet applicable regulatory requirements, GCP standards, and study protocols.
  • Cross-functional partnership: Work closely with clinical development, clinical operations, safety/pharmacovigilance, biostatistics, data management, and regulatory colleagues to resolve issues and support high-quality study execution.
  • Independent judgment: Bring a clear medical perspective to decisions, challenge assumptions when warranted, and know what to escalate and when.

Qualifications and Key Success Factors
  • 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. The position may be hired at the Director or Senior Director level based on the depth and breadth of relevant experience.
  • 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.
  • You'll thrive here if you stay close to the work, communicate clearly, exercise independent judgment, and take ownership. You know when speed matters, when deeper investigation is needed, and when to escalate, all while keeping patient safety at the center.

The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
Compensation & Benefits
At Praxis, we believe that taking care of our people (and their people) is important, so we provide a world class benefits package to help you thrive. This includes 99% of the premium paid for medical, dental and vision plans. We also provide company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. Thinking about the future? We match dollar-for-dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long-term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays and company-wide shutdowns. Not to mention, you'll also be joining a phenomenal crew of colleagues who are smart, engaged and inspiring. We aim high, collaborate hard, and produce results. Let's achieve the impossible together!
To round out our world-class total rewards package, we provide annualized base salary in the range listed below. This range reflects the base salary the Company reasonably expects to pay for the position at the time of posting. Placement within the range will be based on job-related factors, including experience, qualifications, scope of responsibilities, and demonstrated track record of delivering results in similar roles.
Annualized Base Salary
$260,000-$335,000 USD
Compensation & BenefitsAt Praxis, we believe that taking care of our people (and their people) is important, so we provide a world class benefits package to help you thrive. This includes 99% of the premium paid for medical, dental and vision plans. We also provide company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. Thinking about the future? We match dollar-for-dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long-term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays and company-wide shutdowns. Not to mention, you'll also be joining a phenomenal crew of colleagues who are smart, engaged and inspiring. We aim high, collaborate hard, and produce results. Let's achieve the impossible together!
Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
Attention: Job Scam Alert
Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to careers@praxismedicines.com.
Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.