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 ...
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Security Monitoring Associate
Reading, PA · On-site
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Security Monitoring Associate
Reading, PA · On-site
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$157K - $235K/yr
General Summary The Clinical Monitoring Associate Director is responsible for ensuring on-time ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
New
$157K - $235K/yr
General Summary The Clinical Monitoring Associate Director is responsible for ensuring on-time ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
New
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Clinical Monitoring Associate Director
Boston, MA · On-site
$157K - $235K/yr
General Summary The Clinical Monitoring Associate Director is responsible for ensuring on-time ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
New
Clinical Monitoring Associate Director
Boston, MA · On-site
$157K - $235K/yr
General Summary The Clinical Monitoring Associate Director is responsible for ensuring on-time ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
New
Clinical Monitoring Associate Director
Boston, MA · On-site +1
$157K - $235K/yr
The Clinical Monitoring Associate Director is responsible for ensuring on-time monitoring and ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
Clinical Monitoring Associate Director
Boston, MA · On-site +1
$157K - $235K/yr
The Clinical Monitoring Associate Director is responsible for ensuring on-time monitoring and ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
Security Monitoring Associate, Part Time Location: Philadelphia, PA Part Time We are Growers, We ... medical, dental, and vision coverage.
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Clinical Monitoring Associate Director
Boston, MA · On-site
$157K - $235K/yr
The Clinical Monitoring Associate Director is responsible for ensuring on-time monitoring and ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
Clinical Monitoring Associate Director
Boston, MA · On-site
$157K - $235K/yr
The Clinical Monitoring Associate Director is responsible for ensuring on-time monitoring and ... From medical, dental and vision benefits to generous paid time off (including a week-long company ...
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Quick apply
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Medical Monitoring Associate information
See salary details
$24K - $34.1K
15% of jobs
$37.7K is the 25th percentile. Wages below this are outliers.
$34.1K - $44.2K
28% of jobs
The median wage is $49.2K / yr.
$44.2K - $54.3K
14% of jobs
$54.3K - $64.4K
17% of jobs
$65.5K is the 75th percentile. Wages above this are outliers.
$64.4K - $74.5K
12% of jobs
$74.5K - $84.5K
5% of jobs
$84.5K - $94.6K
5% of jobs
$94.6K - $104.7K
3% of jobs
$104.7K - $114.8K
0% of jobs
$114.8K - $124.9K
0% of jobs
$124.9K - $135K
1% of jobs
$24K
$58.4K
$135K
How much do medical monitoring associate jobs pay per year?
As of Sep 13, 2026, the average yearly pay for medical monitoring associate in the United States is $58,439.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,500.00 and $69,500.00 per year, depending on experience, location, and employer.
What is a medical monitoring associate?
Medical Monitoring Associates are professionals who support clinical trials by overseeing the safety of study participants and ensuring that medical data is accurately collected and reported. They work closely with medical monitors, investigators, and clinical research teams to review adverse events, monitor compliance with study protocols, and help resolve medical queries. Their role is vital in maintaining the integrity of clinical trials and ensuring participant safety throughout the research process.
How does a medical monitoring associate typically collaborate with clinical research teams during a study?
Medical Monitoring Associates play a crucial role in ensuring patient safety and data integrity throughout clinical trials. They work closely with clinical research teams by reviewing safety reports, tracking adverse events, and communicating findings to investigators and study sponsors. Collaboration often involves participating in regular team meetings, providing feedback on protocol adherence, and assisting with the preparation of study documentation. This close teamwork ensures that the trial runs smoothly and adheres to regulatory guidelines.
What are the key skills and qualifications needed to thrive as a medical monitoring associate, and why are they important?
To thrive as a Medical Monitoring Associate, you need a solid background in life sciences or nursing, familiarity with clinical trial protocols, and often a relevant degree or certification. Proficiency in clinical data management systems, safety databases, and regulatory compliance tools is typically required. Attention to detail, strong analytical skills, and effective communication are essential soft skills that help ensure accurate medical oversight and teamwork. These competencies are vital to ensure patient safety, regulatory adherence, and the overall integrity of clinical trials.
What cities are hiring for Medical Monitoring Associate jobs?
Cities with the most Medical Monitoring Associate job openings:
What are the most commonly searched types of Medical Monitoring jobs?
The most popular types of Medical Monitoring jobs are:
What are popular job titles related to Medical Monitoring Associate jobs?
For Medical Monitoring Associate jobs, the most frequently searched job titles are:
Director, Medical Monitoring
Lexington, MA • On-site
Kiniksa Pharmaceuticals
• Biotechnology Research and Development • 201 - 500 employees201 - 500 employees
Full-time
Re-posted 10 days ago
Job description
Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, with a focus on cardiovascular indications. With deep expertise in immunology and inflammation, Kiniksa is advancing a growing portfolio of approved and investigational medicines, anchored by its lead product, ARCALYST®, the first and only FDA-approved therapy for recurrent pericarditis. Grounded in rigorous science and bold innovation, the company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders. At Kiniksa, talented individuals are trusted and empowered to make a real impact-shaping the future of medicine while improving the lives of patients who need it most.
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 accordance with Good Clinical Practice (GCP). This role operates as a key contributor, ensuring high quality medical review and timely assessments supporting medical decision support and program execution
This role is based in our Lexington, MA office and requires employees to be onsite five days per week.
Responsibilities (including, but not limited to):
Standout Skills for Impact:
Qualifications and Experience:
Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.
Pay Range
$286,000-$316,000 USD
Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Kiniksa does not accept unsolicited resumes from staffing agencies or search firms. Any resumes submitted without a signed agreement will be considered property of Kiniksa, and no fees will be paid.
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 accordance with Good Clinical Practice (GCP). This role operates as a key contributor, ensuring high quality medical review and timely assessments supporting medical decision support and program execution
This role is based in our Lexington, MA office and requires employees to be onsite five days per week.
Responsibilities (including, but not limited to):
- Provide ongoing medical monitoring oversight for assigned clinical trials, including real-time review of safety data, adverse events, data listings, protocol deviations, eligibility, and laboratory findings to ensure data quality
- Serve as a medical point of contact for investigators and sites on eligibility, protocol interpretation, and participant management questions, including providing medical support for routine medical inquiries from internal and external study teams and sites
- Engage with investigators, advisors, and external experts to support trial execution and clinical oversight
- In collaboration with Global Medical Safety, review and assess adverse events and serious adverse events, including causality assessment, and support safety signal detection in partnership with Pharmacovigilance
- Provide clinical input into protocol design, amendments, informed consent forms, and other study-related documents
- Review and interpret clinical and safety data to inform potential protocol adjustments and trial-level decisions
- Develop and maintain medical monitoring plans and safety review processes for assigned studies in collaboration with Global Medical Safety
- Partner closely with Clinical Operations and CRO on trial conduct, site management, and medical monitoring activities, including leading and supporting discussions with Data Monitoring Committees (DMC)
- Partner with Biometrics and Regulatory Affairs to ensure clinical data support statistical and regulatory requirements
- Collaborate closely with cross-functional team, including Program Management, Medical Safety/Pharmacovigilance, Regulatory Affairs, Biometrics, Medical Affairs, and CMC teams
- Contribute to safety reports, DSURs, and responses to health authority questions
- Provide clinical input into briefing documents, responses to regulatory questions, and clinical components of submissions
- Document all medical monitoring activities and communications related to assigned studies in TMF
- Support preparation for and participate as applicable in site initiation visits and investigator meetings
Standout Skills for Impact:
- Clear and credible communication skills with investigators, cross-functional teams, senior management
- Ability to anticipate enrollment and endpoint challenges before they arise
- Proactive approach in identifying trends early and defining mitigation strategies rather than reacting to problems
- Personable ability to build constructive relationships with investigators and study team
- Ability to handle difficult conversations around protocol deviations, eligibility decisions, and safety events diplomatically
Qualifications and Experience:
- 5+ years of clinical development and/or medical monitoring experience in biotechnology and/or pharmaceutical organizations, with an MD degree; prior experience as a practicing physician is preferred
- Hands-on medical monitoring experience in Phase 2-3 clinical trials
- Experience supporting programs through key clinical trial milestones (e.g., study start-up, interim analyses, pivotal study conduct)
- Strong ability to integrate clinical, safety, and scientific data into sound clinical and risk-benefit decisions
- Solid understanding of global clinical development, GCP, and patient safety requirements
- Familiarity with regulatory submissions (e.g., NDA, BLA, MAA) and support of health authority interactions
- Comfortable operating as an individual contributor in a lean, dynamic environment
- Models transparency, collaboration, and patient-centric decision-making
- Ability to travel domestically and internationally up to 20% for purposes such as site visits and investigator meetings
Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks.
Pay Range
$286,000-$316,000 USD
Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Kiniksa does not accept unsolicited resumes from staffing agencies or search firms. Any resumes submitted without a signed agreement will be considered property of Kiniksa, and no fees will be paid.
About Kiniksa Pharmaceuticals
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
201 - 500 Employees
Headquarters location
Lexington, MA, US
Year founded
2015