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Medical Monitor Cro Jobs (NOW HIRING)

Prometrika LLC

Manager, Medical Writing

Cambridge, MA · On-site

$136K - $164K/yr

PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in ... monitor, and other team members * Clinical sections of INDs, NDAs/BLAs and MAAs and other ...

Fortrea

$240K - $340K/yr

Industry experience inclusive of clinical trials medical monitoring experience or other relevant clinical development/trial experience at a CRO, pharmaceutical company, regulatory agency * Strong ...

Mammoth Biosciences

Senior Clinical Scientist

Brisbane, CA · On-site

$142K - $178K/yr

The incumbent will collaborate closely with the medical monitor, operations team, CRO partner, and study sites to ensure an efficient recruitment and follow-up of subjects in accordance with study ...

CTI

Vice President, Global Medical Affairs

Raleigh, NC · On-site +1

What You'll Bring: * 10 years of progressive experience in the CRO, pharmaceutical or biotech industry. * Significant clinical research experience including medical monitoring. * Deep scientific ...

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Medical Monitor Cro information

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How much do medical monitor cro jobs pay per hour?

As of Jun 30, 2026, the average hourly pay for medical monitor cro in the United States is $44.26, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $57.69 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Monitor in a CRO, and why are they important?

To thrive as a Medical Monitor in a CRO, you need an advanced medical degree (e.g., MD), clinical research experience, and a strong understanding of GCP and regulatory requirements. Familiarity with clinical trial management systems (CTMS), safety databases, and pharmacovigilance tools is typically required. Excellent analytical thinking, attention to detail, and effective communication are crucial soft skills for success in this role. These competencies ensure patient safety, data integrity, and smooth coordination between sponsors, sites, and study teams.

How does a Medical Monitor at a CRO typically interact with study sites and clinical teams during a trial?

A Medical Monitor at a CRO (Contract Research Organization) plays a central role in overseeing the medical aspects of clinical trials, collaborating closely with study site staff, investigators, and other clinical teams. They provide medical guidance, review safety data, and address any protocol deviations or adverse events as they arise. Regular communication—via calls, emails, and meetings—with site personnel ensures patient safety and data integrity throughout the study. This collaboration is essential for troubleshooting issues promptly and maintaining compliance with regulatory requirements.

What is the difference between Medical Monitor Cro vs Medical Monitor?

AspectMedical Monitor CroMedical Monitor
CredentialsMedical degree, relevant clinical experience, often regulatory trainingMedical degree, clinical experience, regulatory knowledge
Work EnvironmentClinical trial sites, CRO offices, regulatory agenciesPharmaceutical companies, CROs, clinical research settings
Employer & IndustryContract Research Organizations (CROs), pharmaceutical industryPharmaceutical companies, CROs, biotech firms
Common Search/ComparisonMedical Monitor Cro vs Medical Monitor

The Medical Monitor Cro and Medical Monitor roles share similar credentials and work environments, often overlapping in clinical trial oversight within CROs and pharmaceutical companies. The main difference lies in their employment context: Medical Monitor Cro typically works within CROs on multiple client projects, while Medical Monitors may be employed directly by pharmaceutical companies. Both roles require medical expertise and regulatory knowledge, but their specific responsibilities and organizational settings differ slightly.

What is a Medical Monitor in clinical research?

A Medical Monitor in clinical research, often employed by a Contract Research Organization (CRO), is a physician responsible for overseeing the safety and well-being of study participants during a clinical trial. They review clinical data, assess adverse events, and provide medical guidance throughout the trial to ensure compliance with regulatory requirements and good clinical practice. Medical Monitors also collaborate with investigators and sponsors to address medical questions and ensure that the study is conducted ethically and safely.
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What states have the most Medical Monitor Cro jobs? States with the most job openings for Medical Monitor Cro jobs include:
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Medical Monitor Cro jobs near you
Associate Medical Director, Clinical Development

Associate Medical Director, Clinical Development

Viridian Therapeutics, Inc.

Waltham, MA • On-site

$230K - $265K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago

Key responsibilities

  • Assist Clinical Development Lead(s) on assigned clinical program and trials.

  • Provide medical oversight as medical monitor on assigned trials and serve as the Sponsor's medical representative to vendors and collaborators.

  • Contribute to the clinical content and review of clinical and regulatory documents, including protocols, INDs, CTAs, investigator brochures, and clinical study reports.

Job description

Description
At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.
Reporting to the VP, Clinical Development, the Associate Medical Director, Clinical Development will support all aspects of clinical development (science and medical), including the generation and review of critical trial-related documents (e.g., investigator brochures, protocols, clinical study reports), contributing to regulatory submissions, and serving as the medical monitor for assigned studies.
This role can be fully remote or based in our Waltham, MA headquarters. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.
Responsibilities (including, but not limited to):
  • Assist Clinical Development Lead(s) on assigned clinical program/ trials
  • Support the development of clinical trial strategies, study designs and scientific strategy
  • Contribute to the clinical content of clinical and regulatory documents, including but not limited to protocols, INDs, CTAs, investigator brochures, CSR's; participate in review SAPs, TLF shells, emerging clinical trial data and data interpretation
  • Provide medical oversight as medical monitor on assigned trials and the Sponsor's medical representative to multiple vendors and collaborators
  • Contribute to preparation and interactions with regulatory authorities
  • Contribute to overall review of clinical data including data listings review in collaboration with Safety/PV, cross-functional teams and engaged vendors
  • Support activities associated with execution of clinical trials and data collection, including training of the internal team, vendors, and site staff; preparation of case report forms; review of protocol deviations; and resolution of issues
  • Partner closely with clinical operations, biostatistics, safety/PV, data management, program management, and research colleagues
  • Support management of DSMB activities
  • Stay current with GCP and worldwide regulatory requirements

Requirements
  • Requires a Medical Degree (MD or equivalent)
  • 3+ years relevant clinical development experience in the biotechnology or pharmaceutical industry; Immunology or Ophthalmology experience is a plus
  • Experience in multiple phases of clinical development desirable
  • Knowledge of FDA regulatory requirements, clinical research concepts & practices, and ICH/GCP guidelines
  • Ability for creative problem-solving, strategic thinking, risk identification & mitigation skills
  • Team-oriented and works collaboratively with cross-functional teams
  • Ability to demonstrate flexibility and adaptability in a dynamic environment
  • Experience working with and managing third party vendors, such as CRO's
  • Strong oral and written communication skills
  • Excellent interpersonal/ organizational skills with the ability to multi-task
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • Ability to travel up to 20%
  • The salary range for this position is commensurate with experience

Viridian offers a comprehensive benefits package including:
  • Competitive pay and stock options for all employees
  • Medical, dental, and vision coverage
  • Fertility and mental health programs
  • Short- and long-term disability coverage
  • Life, Travel and AD&D
  • 401(k) Company Match with immediate company vest
  • Employee Stock Purchase plan
  • Generous vacation plan and paid company holiday shutdowns
  • Various mental, financial, and proactive physical health programs covered by Viridian

Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian 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.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.

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