Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Quick apply
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Design and implement safety monitoring plans * DBL (final listing review, review of blinded TLF ... work with medical writer to review & revise CSR document, draft discussion and conclusions ...
Design and implement safety monitoring plans * DBL (final listing review, review of blinded TLF ... work with medical writer to review & revise CSR document, draft discussion and conclusions ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Quick apply
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Quick apply
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
Quick apply
Responsible for medical monitoring tasks * Provide medical input throughout the development process * Provide medical input into the development and execution of study documents and plans, such as ...
As the medical and scientific authority for one or more studies, you will be fully accountable for study design, execution, monitoring, delivery, and reporting, partnering closely with cross ...
As the medical and scientific authority for one or more studies, you will be fully accountable for study design, execution, monitoring, delivery, and reporting, partnering closely with cross ...
... medical monitoring, and regulatory engagement. This role is ideally suited for someone with direct ... hands-on leadership experience in early-phase clinical trials within pharmaceutical or ...
... medical monitoring, and regulatory engagement. This role is ideally suited for someone with direct ... hands-on leadership experience in early-phase clinical trials within pharmaceutical or ...
The Medical Monitor will be responsible for patient safety oversight, protocol implementation, investigator engagement, medical review of efficacy and safety data, and contribution to regulatory ...
The Medical Monitor will be responsible for patient safety oversight, protocol implementation, investigator engagement, medical review of efficacy and safety data, and contribution to regulatory ...
... medical monitoring, and regulatory engagement. This role is ideally suited for someone with direct ... hands-on leadership experience in early-phase clinical trials within pharmaceutical or ...
... medical monitoring, and regulatory engagement. This role is ideally suited for someone with direct ... hands-on leadership experience in early-phase clinical trials within pharmaceutical or ...
Medical Director/Senior Medical Director, Clinical Development
$300K - $390K/yr
Serves as the medical monitor for clinical trials and assists in resolving major issues that may affect their assigned studies. * Partners with the Clinical Scientist, Data Manager, Pharmacovigilance ...
Medical Director/Senior Medical Director, Clinical Development
$300K - $390K/yr
Serves as the medical monitor for clinical trials and assists in resolving major issues that may affect their assigned studies. * Partners with the Clinical Scientist, Data Manager, Pharmacovigilance ...
As a Medical Director at Parexel, you will provide medical monitoring for assigned projects, function as medical representative on the project team, provide medical consultation as required or ...
As a Medical Director at Parexel, you will provide medical monitoring for assigned projects, function as medical representative on the project team, provide medical consultation as required or ...
Vice President, Global Medical Affairs
Covington, KY · On-site +1
Provide executive medical oversight across global clinical trials (Phases I-IV). * Oversee medical monitoring activities including development and review of Medical Monitoring Plans. * Ensure ...
Vice President, Global Medical Affairs
Covington, KY · On-site +1
Provide executive medical oversight across global clinical trials (Phases I-IV). * Oversee medical monitoring activities including development and review of Medical Monitoring Plans. * Ensure ...
Senior Medical Director
San Francisco, CA · On-site
$325K - $400K/yr
This individual will serve as the medical monitor and cross-functional medical lead for assigned programs, ensuring scientific rigor, patient safety, and high-quality data generation while working ...
Senior Medical Director
San Francisco, CA · On-site
$325K - $400K/yr
This individual will serve as the medical monitor and cross-functional medical lead for assigned programs, ensuring scientific rigor, patient safety, and high-quality data generation while working ...
Provide medical review and medical monitoring for Phase 2 and Phase 3 studies (in partnership with CRO medical monitors). * Participate in strategic discussions on clinical development plans ...
Provide medical review and medical monitoring for Phase 2 and Phase 3 studies (in partnership with CRO medical monitors). * Participate in strategic discussions on clinical development plans ...
Senior Medical Director
San Francisco, CA · Remote
$325K - $400K/yr
This individual will serve as the medical monitor and cross-functional medical lead for assigned programs, ensuring scientific rigor, patient safety, and high-quality data generation while working ...
Senior Medical Director
San Francisco, CA · Remote
$325K - $400K/yr
This individual will serve as the medical monitor and cross-functional medical lead for assigned programs, ensuring scientific rigor, patient safety, and high-quality data generation while working ...
Vice President, Global Medical Affairs
Covington, KY · On-site +1
Provide executive medical oversight across global clinical trials (Phases I-IV). * Oversee medical monitoring activities including development and review of Medical Monitoring Plans. * Ensure ...
Vice President, Global Medical Affairs
Covington, KY · On-site +1
Provide executive medical oversight across global clinical trials (Phases I-IV). * Oversee medical monitoring activities including development and review of Medical Monitoring Plans. * Ensure ...
Senior Medical Director
Seattle, WA · On-site
$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 ...
Senior Medical Director
Seattle, WA · On-site
$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 ...
Medical Monitoring information
See salary details
$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
How much do medical monitoring jobs pay per year?
As of Jun 30, 2026, the average yearly pay for medical monitoring in the United States is $92,555.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,500.00 and $84,500.00 per year, depending on experience, location, and employer.
What is a Medical Monitoring job?
A Medical Monitoring job involves overseeing the safety and integrity of clinical trials by assessing adverse events, ensuring protocol compliance, and providing medical oversight. Professionals in this role, often physicians or healthcare experts, collaborate with clinical teams to evaluate patient safety data and regulatory reporting requirements. They play a crucial role in ensuring that trial participants are protected while maintaining the scientific validity of the study.
What are the key skills and qualifications needed to thrive in the Medical Monitoring position, and why are they important?
To thrive in Medical Monitoring, a strong background in clinical practice or life sciences, attention to detail, and critical thinking are essential, often supported by a relevant medical or scientific degree. Familiarity with safety databases, adverse event reporting systems, and tools for data analysis, as well as certifications such as GCP (Good Clinical Practice), are commonly required. Effective communication, decisiveness, and the ability to collaborate across multidisciplinary teams help individuals excel in this role. These skills ensure the accurate monitoring of clinical trials and patient safety, supporting compliance and the integrity of medical research.
What are the typical day-to-day responsibilities of someone working in Medical Monitoring?
In a Medical Monitoring role, your daily responsibilities often include reviewing data from ongoing clinical trials, assessing adverse event reports, providing medical expertise to study teams, and ensuring that patient safety is maintained throughout the research process. You may participate in meetings with investigators, contribute to protocol development, and respond to safety concerns as they arise. Collaboration with clinical research associates, data managers, regulatory personnel, and sponsors is common, requiring clear and timely communication. This role is integral to maintaining trial integrity, regulatory compliance, and ensuring participant well-being.
More about Medical Monitoring jobs
What cities are hiring for Medical Monitoring jobs? Cities with the most Medical Monitoring job openings:
What are the most commonly searched types of Medical Monitoring jobs? The most popular types of Medical Monitoring jobs are:
What states have the most Medical Monitoring jobs? States with the most job openings for Medical Monitoring jobs include:
What job categories do people searching Medical Monitoring jobs look for? The top searched job categories for Medical Monitoring jobs are:
Part-time
Posted 24 days ago
Key responsibilities
Provide medical expertise on development-related or emerging cardiac safety concerns.
Serve as primary medical reviewer of individual adverse event reports, clinical, and safety documents.
Lead safety activities on assigned product(s) including interactions with other functional groups.
Job description
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This role is a project-based consulting opportunity to conduct medical reviewing on an as-needed basis. This is not a full-time position.
Roles & Responsibilities
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This role is a project-based consulting opportunity to conduct medical reviewing on an as-needed basis. This is not a full-time position.
Roles & Responsibilities
- Provide medical expertise on development-related or emerging cardiac safety concerns
- Responsible for medical monitoring tasks
- Provide medical input throughout the development process
- Provide medical input into the development and execution of study documents and plans, such as study protocol, IB, SMP, DMP, SAP, Lab manuals, etc.
- Provide significant expertise as primary medical reviewer of individual adverse event reports, clinical, and safety documents
- Lead safety activities on assigned product(s) that may include interactions with other functional groups in the company
- Responsible for strategies in pre and post marketing risk management, as well as keeping abreast of pharmacovigilance methods and trends in published literature and global regulations
- Responsible for strategies in monitoring and analysis of cumulative safety information
- Maintains significant knowledge of global and local regulations and guidance as they pertain to medical review and safety reporting
- Medical degree required (MD or equivalent)
- Specialty in Cardiology or comparable experience in Cardiology
- 5 or more years of clinical experience and/ or research experience required
- Relevant experience in medical monitoring and/or medical reviewer in pharmaceutical industry
- Excellent scientific writing skills
- Ability to understand clinical data
- Proficiency with MS Office applications
- Good communication skills
- Strong knowledge of current regulatory practices and domestic and international regulations
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About M. M. S.
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1 - 10 Employees
Headquarters location
Los Angeles, CA, US
Year founded
1980