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Medical Monitor Jobs in Boston, MA (NOW HIRING)

Cugene Inc.

Medical Monitor

Boston, MA · On-site

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 ...

New

Cugene Inc.

Medical Monitor

Boston, MA · On-site

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 ...

New

Icon plc

Medical Director

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 ...

AVEO Oncology

Medical Director

Boston, MA · Remote

... Monitoring and Safety Oversight: · Serve as the medical monitor for assigned clinical trials, providing ongoing medical oversight and guidance, addressing any issues that arise to ensure timely ...

AVEO Oncology

Medical Director

Boston, MA · On-site

... Monitoring and Safety Oversight: • Serve as the medical monitor for assigned clinical trials, providing ongoing medical oversight and guidance, addressing any issues that arise to ensure timely ...

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Medical Monitor information

See Boston, MA salary details

$22.8K

$100.5K

$193.4K

How much do medical monitor jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical monitor in Boston, MA is $100,547.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,800.00 and $91,800.00 per year, depending on experience, location, and employer.

What is a medical monitor?

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.

What are the typical daily responsibilities of a medical monitor in a clinical research setting?

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.

What are the key skills and qualifications needed to thrive in the medical monitor position, and why are they important?

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.

What are the most commonly searched types of Medical Monitor jobs in Boston, MA?

The most popular types of Medical Monitor jobs in Boston, MA are:

What are popular job titles related to Medical Monitor jobs in Boston, MA?

For Medical Monitor jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Medical Monitor jobs in Boston, MA look for?

The top searched job categories for Medical Monitor jobs in Boston, MA are:

Medical Monitor jobs near you
Infographic showing various Medical Monitor job openings in Boston, MA as of August 2026, with employment types broken down into 67% Full Time, 20% Part Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $100,547 per year, or $48.3 per hour.

Medical Monitor

Cugene Inc.

Boston, MA • On-site

Other

Posted 2 days ago

New

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. 

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About Cugene

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

11 - 50 Employees

Headquarters location

Waltham, MA, US

Year founded

2016

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