Monitor Technician
Waterloo, IA · On-site
Using hospital equipment and medical technology to perform various tests on patients' hearts, such ... Cleaning and maintaining heart monitors and EKG machines. * Reporting any necessary equipment ...
Waterloo, IA · On-site
Using hospital equipment and medical technology to perform various tests on patients' hearts, such ... Cleaning and maintaining heart monitors and EKG machines. * Reporting any necessary equipment ...
Waterloo, IA · On-site
Using hospital equipment and medical technology to perform various tests on patients' hearts, such ... Cleaning and maintaining heart monitors and EKG machines. * Reporting any necessary equipment ...
The Director, Medical Monitoring, is a key role responsible for ensuring appropriate medical oversight in conducting the study protocol including the integrity of assigned clinical studies in ...
The Director, Medical Monitoring, is a key role responsible for ensuring appropriate medical oversight in conducting the study protocol including the integrity of assigned clinical studies in ...
Serve as medical monitor for ongoing clinical trials, ensuring patient safety and data integrity. * Review and interpret clinical data, including safety and efficacy endpoints. * Cross-Functional ...
Serve as medical monitor for ongoing clinical trials, ensuring patient safety and data integrity. * Review and interpret clinical data, including safety and efficacy endpoints. * Cross-Functional ...
Medical Monitor for the assigned trials or studies * Medical Data Review * Protocol development from concept to final protocol * Protocol execution including interaction with investigators, and ...
Medical Monitor for the assigned trials or studies * Medical Data Review * Protocol development from concept to final protocol * Protocol execution including interaction with investigators, and ...
Medical Monitor for the assigned trials or studies * Medical Data Review * Protocol development from concept to final protocol * Protocol execution including interaction with investigators, and ...
Medical Monitor for the assigned trials or studies * Medical Data Review * Protocol development from concept to final protocol * Protocol execution including interaction with investigators, and ...
Ithaca, NY · On-site
Ultimately, a top-notch monitor technician should have a strong working knowledge of medical equipment and software, as well as good communication skills when interacting with patients. Monitor ...
Ithaca, NY · On-site
Ultimately, a top-notch monitor technician should have a strong working knowledge of medical equipment and software, as well as good communication skills when interacting with patients. Monitor ...
This position is more of a tactical medical monitoring clinical data review role. This opportunity is with a small pharmaceutical company in the Boston area. A hands- position working as a medical ...
This position is more of a tactical medical monitoring clinical data review role. This opportunity is with a small pharmaceutical company in the Boston area. A hands- position working as a medical ...
Boston, MA · On-site
$185 - $277/hr
Medical Monitor for the assigned trials or studies* Medical Data Review* Protocol development from concept to final protocol* Protocol execution including interaction with investigators, and ...
Boston, MA · On-site
$185 - $277/hr
Medical Monitor for the assigned trials or studies* Medical Data Review* Protocol development from concept to final protocol* Protocol execution including interaction with investigators, and ...
$323K - $381K/yr
This position serves as a responsible medical monitor or a Lead medical monitor for various clinical phase 1 - 3 trials, as needed. * Uses medical/scientific expertise to create or support the ...
$323K - $381K/yr
This position serves as a responsible medical monitor or a Lead medical monitor for various clinical phase 1 - 3 trials, as needed. * Uses medical/scientific expertise to create or support the ...
Princeton, NJ · On-site
$323K - $381K/yr
This position serves as a responsible medical monitor or a Lead medical monitor for various clinical phase 1 - 3 trials, as needed. * Uses medical/scientific expertise to create or support the ...
Princeton, NJ · On-site
$323K - $381K/yr
This position serves as a responsible medical monitor or a Lead medical monitor for various clinical phase 1 - 3 trials, as needed. * Uses medical/scientific expertise to create or support the ...
Rockville, MD · Remote
Cooperates directly with Safety Monitors, Project Leadership, Data Managers and other relevant functional groups. * At the project level, will function in the role of a Medical Monitor leading the ...
Rockville, MD · Remote
Cooperates directly with Safety Monitors, Project Leadership, Data Managers and other relevant functional groups. * At the project level, will function in the role of a Medical Monitor leading the ...
$270K - $333K/yr
Serve as medical monitor for clinical studies, ensuring patient safety, data integrity, and compliance with GCP and regulatory requirements. * Lead preparation of clinical protocols, investigator ...
$270K - $333K/yr
Serve as medical monitor for clinical studies, ensuring patient safety, data integrity, and compliance with GCP and regulatory requirements. * Lead preparation of clinical protocols, investigator ...
Palo Alto, CA · On-site
$250 - $350/hr
Serve as a Medical Monitor for clinical trials, ensure study integrity, and track accumulating safety and efficacy data * Provide leadership to study teams * Ensure successful completion of ...
Palo Alto, CA · On-site
$250 - $350/hr
Serve as a Medical Monitor for clinical trials, ensure study integrity, and track accumulating safety and efficacy data * Provide leadership to study teams * Ensure successful completion of ...
Independently provide medical monitor support to assigned clinical studies, for example answering medical questions from study team and/or site, assist with protocol interpretation and medical review ...
Independently provide medical monitor support to assigned clinical studies, for example answering medical questions from study team and/or site, assist with protocol interpretation and medical review ...
Independently provide medical monitor support to assigned clinical studies, for example answering medical questions from study team and/or site, assist with protocol interpretation and medical review ...
Independently provide medical monitor support to assigned clinical studies, for example answering medical questions from study team and/or site, assist with protocol interpretation and medical review ...
Durham, NC · Remote
$154K - $431K/yr
Medical Monitoring: * Primarily serves as Medical Monitor (at the global or regional level) on assigned clinical trials. * Serves as Scientific Advisor (providing medical advice and input) to Project ...
Durham, NC · Remote
$154K - $431K/yr
Medical Monitoring: * Primarily serves as Medical Monitor (at the global or regional level) on assigned clinical trials. * Serves as Scientific Advisor (providing medical advice and input) to Project ...
Cambridge, MA · On-site
Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs. * Contribute directly to the authoring of protocols ...
Quick apply
Cambridge, MA · On-site
Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs. * Contribute directly to the authoring of protocols ...
Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs. * Contribute directly to the authoring of protocols ...
Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs. * Contribute directly to the authoring of protocols ...
Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs. * Contribute directly to the authoring of protocols ...
Quick apply
Serve as the Global Clinical Lead and Medical Monitor for one or more studies, including participation on the clinical sub-teams of those programs. * Contribute directly to the authoring of protocols ...
Cambridge, MA · On-site
Medical Monitoring: Serve as Medical Monitor for Phase III and registration trials, ensuring patient safety, protocol compliance, and timely medical oversight. Review safety data, support data ...
Cambridge, MA · On-site
Medical Monitoring: Serve as Medical Monitor for Phase III and registration trials, ensuring patient safety, protocol compliance, and timely medical oversight. Review safety data, support data ...
$21K - $35.3K
4% of jobs
$35.3K - $49.5K
2% of jobs
$49.5K - $63.8K
1% of jobs
$63.8K - $78.1K
0% of jobs
$81.1K is the 25th percentile. Wages below this are outliers.
$78.1K - $92.4K
82% of jobs
$92.4K - $106.6K
3% of jobs
$106.6K - $120.9K
6% of jobs
$120.9K - $135.2K
0% of jobs
$135.2K - $149.5K
0% of jobs
$149.5K - $163.7K
0% of jobs
$163.7K - $178K
1% of jobs
$21K
$92.6K
$178K
To thrive as a Medical Monitor, you need a deep understanding of clinical research, medical evaluation, and regulatory compliance, typically supported by a medical degree (MD or equivalent) and clinical experience. Familiarity with clinical trial management systems (CTMS), safety databases, and Good Clinical Practice (GCP) certification is essential. Excellent communication, analytical thinking, and problem-solving skills help you clearly communicate findings and collaborate with cross-functional teams. These competencies are vital to ensure participant safety, data integrity, and the smooth conduct of clinical trials.
A Medical Monitor is a physician responsible for ensuring the safety and integrity of clinical trials. They provide medical oversight by reviewing patient data, assessing adverse events, and ensuring compliance with regulatory guidelines. Medical Monitors work closely with clinical teams, investigators, and regulatory agencies to support the study's progress and ethical conduct. Their expertise helps ensure that trials meet safety standards while gathering reliable data for drug development.
As a Medical Monitor, your daily responsibilities often include reviewing adverse event reports, monitoring patient safety data, and providing medical input during clinical trial meetings. You will interpret clinical data, ensure protocol adherence, and address any medical queries from site staff or sponsors. Additionally, you collaborate closely with clinical operations, safety, and regulatory teams to ensure trials are conducted safely and efficiently. This role requires ongoing communication with investigators and the ability to rapidly assess and respond to potential safety concerns.

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Posted 15 days ago