ZipRecruiter

Log In

1

Research Medical Monitor Jobs (NOW HIRING)

Cugene Inc.

Medical Monitor

Boston, MA · On-site

This individual will work closely with the Head of R&D and cross‑functional teams to advance the ... ICF, medical monitoring plans, safety narratives, DSURs, and statical analysis plan and data ...

ICON Clinical Research

Medical Monitor

Lenexa, KS · On-site

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 ...

ICON

Medical Monitor

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 ...

410 ICR United States USA

Medical Monitor

United, PA · On-site

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 ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Strong understanding of clinical research, ICH-GCP, FDA, EMA, and other applicable regulatory ...

next page

Showing results 1-20

All JobsHealthcare JobsMedical Research JobsMedical Researcher JobsResearch Medical Monitor Jobs

Research Medical Monitor information

See salary details

$37.5K

$53.3K

$58.5K

How much do research medical monitor jobs pay per year?

As of Sep 11, 2026, the average yearly pay for research medical monitor in the United States is $53,326.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $58,000.00 per year, depending on experience, location, and employer.

What is a research medical monitor?

A Research Medical Monitor is a physician or healthcare professional responsible for overseeing the safety and integrity of clinical trials. They review study protocols, assess adverse events, and ensure that participants' well-being is protected throughout the research process. Their role involves providing medical expertise, monitoring data, and ensuring compliance with regulatory and ethical standards. The Research Medical Monitor acts as a liaison between the clinical investigators, sponsors, and regulatory authorities to ensure that the study is conducted safely and effectively.

What are the key skills and qualifications needed to thrive as a research medical monitor?

To thrive as a Research Medical Monitor, you need a medical degree (MD or equivalent), strong clinical research knowledge, and experience in drug safety and regulatory compliance. Familiarity with clinical trial management systems, pharmacovigilance databases, and Good Clinical Practice (GCP) guidelines is typically required. Exceptional analytical thinking, attention to detail, and effective communication skills help you collaborate with study teams and ensure participant safety. These competencies are crucial for maintaining ethical standards, ensuring regulatory adherence, and safeguarding subjects during clinical trials.

What are some common challenges faced by research medical monitors, and how can they be addressed?

Research Medical Monitors often face challenges such as ensuring protocol compliance across multiple study sites, managing large volumes of safety data, and maintaining clear communication among cross-functional teams. To address these challenges, it’s important to establish robust processes for data review, participate in regular team meetings, and leverage technology for efficient safety reporting. Building strong relationships with investigators and site staff also helps in quickly resolving protocol deviations and ensuring participant safety throughout the clinical trial.

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

AspectResearch Medical Monitor

The Research Medical Monitor and Clinical Research Associate (CRA) both work in clinical trials, but their roles differ significantly. The Research Medical Monitor primarily oversees patient safety, reviews data, and ensures compliance with protocols, often requiring medical credentials. The CRA manages site activities, monitors trial progress, and ensures data accuracy, typically without medical degrees. Both roles are essential in clinical research, but the Medical Monitor has a more clinical and safety-focused responsibility, while the CRA handles operational tasks.

What cities are hiring for Research Medical Monitor jobs?

Cities with the most Research Medical Monitor job openings:

What states have the most Research Medical Monitor jobs?

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

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

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

Research Medical Monitor jobs near you
Infographic showing various Research Medical Monitor job openings in the United States as of June 2026, with employment types broken down into 40% Full Time, 39% Part Time, 1% Temporary, 19% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $53,326 per year, or $25.6 per hour.

Medical Monitor

Boston, MA • On-site

Cugene Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about Cugene Inc.external

Other

This job post has expired today. Applications are no longer accepted.

Job description

Company Description CUGENE Inc. is a clinical-stage biotechnology company dedicated to the discovery and development of innovative medicines for the treatment of cancer and autoimmune diseases. Guided by our mission to improve lives, we harness the power of the immune system to combat disease.

We are committed to fostering a diverse, inclusive, and ethical environment where innovation, integrity, and accountability are central to our culture. We deeply value our people and seek highly skilled, driven individuals who share our passion and commitment. Together, we strive toward one unified vision: One Passion, Many Cures.

Role Description The Medical Monitor will provide medical leadership and oversight for early- to mid-phase clinical trials, with responsibility for patient safety, protocol development, medical decision-making, and regulatory interactions. This individual will work closely with the Head of R&D and cross‑functional teams to advance the clinical pipeline in global trials. The successful candidate will have deep expertise in immunology/autoimmune and immuno-oncology (solid tumor indications) and large-molecule biologics-based therapies. The candidate must be able to thrive in a fast-paced startup environment and has demonstrated experience guiding early clinical programs from first in human through proof of concept.

KEY RESPONSIBILITIES

  • Ensure individual participant’s safety and the scientific integrity of the trials in accordance of the guidance of ICH Good Clinical Practice (GCP), Standard Operating Procedures (SOPs) and local regulatory guidelines
  • Provide real-time medical guidance to the clinical development teams including clinical operations, CROs, investigators, and vendors
  • Provide medical support for routine medical inquiries and on‑call medical support for urgent medical inquiries
  • Review safety information, including adverse events and clinical laboratory data, to inform patient-level medical decisions when necessary
  • Assess and manage immune-mediated toxicities
  • Review medical raw data listings and coding listings, and assess protocol deviations
  • Confirm patient eligibility based on IE criteria and medical history and concomitant medications
  • Implement dose escalation/de‑escalation decisions, stopping rules, and toxicity management plans
  • Assess clinical indications and medical needs in autoimmune and inflammation field, design clinical study and author study protocols
  • Author and/or review key regulatory documents, including the study synopsis, CSRs, IB, CRF, ICF, medical monitoring plans, safety narratives, DSURs, and statical analysis plan and data package
  • Serve as a key clinical point of contact for regulatory agencies and respond to questions related to clinical safety and trial conduct

Qualifications

  • MD or equivalent international medical degree
  • 7+ years of clinical research and drug development experience leading early-phase (Phase I–II) immuno-oncology or autoimmune/inflammation trials with a strong preference for biologics-based immunotherapy in biotech or pharmaceutical settings, including direct medical monitoring responsibility
  • Strong understanding of Immune-related adverse events (irAEs)
  • Strong clinical trial design and execution ability
  • Excellent written and verbal communication
  • Demonstrated ability to work independently and effectively in a team environment

Travel Requirements

  • Willingness and ability to travel domestically and internationally

Why Join Us

  • Opportunity to shape clinical strategy at a critical growth stage
  • High visibility and direct impact on pipeline success
  • Collaborative, science-driven culture with global reach

Qualified candidate will be hired at the appropriate level commensurate with education and experience with proven track records of research accomplishments. 

Cugene logo

About Cugene

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

11 - 50 Employees

Headquarters location

Waltham, MA, US

Year founded

2016

View All Cugene Jobs

Apply