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Medical Monitoring information

See California salary details

$20.7K

$91.3K

$175.7K

How much do medical monitoring jobs pay per year?

As of Jul 26, 2026, the average yearly pay for medical monitoring in California is $91,343.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,400.00 and $83,400.00 per year, depending on experience, location, and employer.

How much do medical monitors make in the US?

Medical monitors in the US typically earn a median annual salary of around $80,000 to $100,000, depending on experience, location, and the complexity of clinical trials. Salaries can range from approximately $60,000 for entry-level roles to over $120,000 for senior positions or those with specialized certifications. The role often requires knowledge of Good Clinical Practice (GCP) and regulatory guidelines.

What is the easiest medical job that pays well?

A medical monitoring role, such as a medical assistant or patient care technician, is generally considered easier to enter and offers decent pay compared to more specialized healthcare positions. These jobs often require a certification or short training program and involve tasks like patient intake, vital signs, and basic clinical support. While pay varies by location, these roles typically provide a good balance of accessibility and compensation in the healthcare field.

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 is a medically monitored position?

A medical monitoring position involves overseeing and ensuring the health and safety of individuals, often in healthcare, clinical, or research settings. It typically requires knowledge of medical protocols, certifications such as CPR or first aid, and the ability to respond quickly to medical emergencies.

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.

How to be a medical monitor?

A medical monitor is a healthcare professional responsible for overseeing clinical trial safety and compliance. To become one, typically a physician or licensed healthcare provider with experience in clinical research is required, along with knowledge of Good Clinical Practice (GCP) guidelines and relevant certifications. Strong communication skills and attention to detail are essential for monitoring patient safety and data integrity throughout a trial.
What are the most commonly searched types of Medical Monitoring jobs in California? The most popular types of Medical Monitoring jobs in California are:
What are popular job titles related to Medical Monitoring jobs in California? For Medical Monitoring jobs in California, the most frequently searched job titles are:
What job categories do people searching Medical Monitoring jobs in California look for? The top searched job categories for Medical Monitoring jobs in California are:
Medical Monitoring jobs near you
Infographic showing various Medical Monitoring job openings in California as of July 2026, with employment types broken down into 70% Full Time, 10% Part Time, and 20% Contract. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $91,343 per year, or $43.9 per hour.
Director / Sr. Director, Medical Monitor

Director / Sr. Director, Medical Monitor

Artiva Biotherapeutics Inc.

San Diego, CA • On-site

$250 - $350/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago

Job description

About Artiva

We are a clinical‑stage biotechnology company focused on developing natural killer (NK) cell‑based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non‑genetically modified, cryopreserved NK cell therapy being evaluated in combination with B‑cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.

For more information, visit www.artivabio.com.

Job Summary

The Senior Director/Sr. Director, Medical Monitor provides medical oversight and safety monitoring across Artiva's clinical trials, ensuring participant safety, data integrity, and regulatory compliance throughout study conduct. This role requires an experienced physician with strong clinical judgment and hands‑on medical monitoring experience in Phase 2‑3 studies, who collaborates effectively across functions while thriving in a fast‑moving biotech environment.

Duties/Responsibilities
  • Provide ongoing medical monitoring and safety oversight for assigned clinical trials, including real‑time review of safety data, adverse events, and laboratory findings.
  • Serve as the primary medical point of contact for investigators and sites on eligibility, protocol interpretation, and patient management questions.
  • Engage with investigators, advisors, and external experts to support trial execution and clinical oversight.
  • Review and assess adverse events and serious adverse events, including causality assessment, and support safety signal detection in partnership with Pharmacovigilance.
  • Conduct ongoing medical and clinical data review, including data listings, protocol deviations, and eligibility, to ensure data quality and participant safety.
  • Provide clinical input into protocols, amendments, informed consent forms, and other study‑related documents.
  • Review and interpret clinical and safety data to inform protocol adjustments and trial‑level decisions.
  • Develop and maintain medical monitoring plans and safety review processes for assigned studies.
  • Partner closely with Clinical Operations and CROs on trial conduct, site management, and medical monitoring activities.
  • Partner with Biometrics and Regulatory Affairs to ensure clinical data supports statistical and regulatory requirements.
  • Collaborate closely with Translational Medicine, Safety/Pharmacovigilance, Regulatory Affairs, Biometrics, Medical Affairs, and CMC teams.
  • Provide clinical input into biomarker and safety strategies.
  • 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.
  • Support readiness for audits, inspections, and regulatory review.
Requirements
  • MD required.
  • Hands‑on medical monitoring experience in Phase 2‑3 clinical trials in rheumatology or immunology indications required.
  • Background in immunology, autoimmune disease, rheumatology or cell therapy required.
  • Rheumatologist with Board certification preferred.
  • 5+ years of clinical development and/or medical monitoring experience in biotechnology and/or pharmaceutical organizations.
  • 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.
  • Clear and credible communicator with investigators, cross‑functional teams, senior management, and external experts.
  • Familiarity with regulatory submissions (e.g., NDA, BLA, MAA) and support of health authority interactions.
  • Comfortable operating as an individual contributor in a lean, fast‑moving biotech environment.
  • Models transparency, collaboration, and patient‑centric decision‑making.
In addition to a great culture, we offer:
  • A beautiful facility
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
    • Medical, Dental, and Vision
    • Group Life Insurance
    • Long Term Disability (LTD)
    • 401(k) Retirement Plan
    • Employee Assistance Program (EAP)
    • Flexible Spending Account (FSA)
    • Paid Time Off (PTO)
    • Company paid holidays, including the year‑end holiday week
    • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.

If all this speaks to you, come join us on our journey!

Base Salary: $250,000 - 350,000. Exact compensation may vary based on skills and experience.

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