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Medical Monitor Cro Jobs (NOW HIRING)

Cartesian Therapeutics

Medical Director

Frederick, MD · Remote

Review subject eligibility, protocol deviations, dose interruptions, and significant safety events in collaboration with the CRO medical monitor and investigative sites * Provide medical oversight ...

IQVIA, Inc.

Medical Director, Rheumatologist

Durham, NC · On-site

$154K - $431K/yr

Medical Monitoring : * Primarily serves as Medical Monitor (at the global or regional level) on ... Pharma, CRO, or Biotech industry. * Ability to establish and maintain effective working ...

IQVIA

Medical Director, Rheumatologist

Durham, NC · Remote

$154K - $431K/yr

Medical Monitoring : * Primarily serves as Medical Monitor (at the global or regional level) on ... Pharma, CRO, or Biotech industry. * Ability to establish and maintain effective working ...

IQVIA

Medical Director, Rheumatologist

Durham, NC · Remote

$154K - $431K/yr

Medical Monitoring : * Primarily serves as Medical Monitor (at the global or regional level) on ... Pharma, CRO, or Biotech industry. * Ability to establish and maintain effective working ...

Pramand LLC

Clinical Trial Manager

Bedford, MA · On-site

Monitor CRO performance metrics and escalate concerns to the Sr. Clinical Operations Manager Budget ... Medical device clinical trial experience strongly preferred * Demonstrated knowledge of FDA ...

Apply Early

Pramand

Clinical Trial Manager

Bedford, MA

$85 - $110/hr

Monitor CRO performance metrics and escalate concerns to the Sr. Clinical Operations Manager Budget ... Medical device clinical trial experience strongly preferred * Demonstrated knowledge of FDA ...

Pramand

Clinical Trial Manager

Bedford, MA · On-site

$85 - $110/hr

Monitor CRO performance metrics and escalate concerns to the Sr. Clinical Operations Manager Budget ... Medical device clinical trial experience strongly preferred * Demonstrated knowledge of FDA ...

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Medical Monitor Cro information

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$14

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$74

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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Medical Monitor Cro jobs near you
Medical Monitor

Medical Monitor

Artech Information System LLC

Lawrence Township, NJ • On-site

Contractor

Posted 15 days ago

Job description

Company Description

Artech is the 10th Largest ITStaffing Company in the US, according to Staffing Industry Analysts' 2012annual report. Artech provides technical expertise to fill gaps in clients'immediate skill-sets availability, deliver emerging technology skill-sets,refresh existing skill base, allow for flexibility in project planning andexecution phases, and provide budgeting/financial flexibility by offeringcontingent labor as a variable cost. 

Job Description

Job Description

  • Clinical Trial Medical Monitor

Role Imperatives

  • Work with Clinical Trial Lead/Program Lead or Early Asset Development Lead and cross functional study team to monitor and clean ongoing oncology studies, and support database locks.
  • Work with the clinical team to review the safety data using different tools: J-Review, CIOMS and CFR imaging tools.

Essential Core Behaviors

  • Ability to work and communicate efficiently with internal partners
  • Working effectively in a matrix organization
  • Ability to work independently

Desired Background, Knowledge, And Experience

  • MD or DO with experience in Oncology
  • A minimum of 3 - 5 years of industry experience
  • In depth knowledge of and experience as a medical monitor for clinical trials (Phase I - III)
  • Good verbal and written communication skills essential
  • Experience managing projects in a matrix environment, coordinating activities and adhering to tight timelines
  • Excellent written and verbal communication skills are required
  • Attend weekly update meeting with BMS core team (PM, DM, stats, CRO) as required
  • Respond to site and Health Authority questions about the protocol
  • Weekly investigator calls for Phase I studies as needed
  • Monthly review of Jreview and CRO data listings and QNET lab data. Attend monthly safety meetings
  • Review daily lab alerts and SAEs. Communicate with CRO sites regarding follow-up.
  • Monthly review of protocol deviations
  • Attend and present at Investigator meetings
  • CRF review
  • Present study updates as needed
  • Design and implement safety monitoring plans
  • DBL (final listing review, review of blinded TLF, review protocol deviations, participate in all DBL meetings)
  • CSR writing (review final TLFs, work with medical writer to review & revise CSR document, draft discussion and conclusions, participate in comment resolution meetings)
  • Topline results presentation
  • Other tasks may be required as determined during the project by BMS
  • The position is preferably based in the Princeton, NJ area but working remotely with occasional face to face meeting acceptable depending on business needs. Will need to be present in NJ for initial onboarding/training.
Qualifications
  • MD or DO with experience in Oncology
  • A minimum of 3 - 5 years of industry experience
Additional Information

All your information will be kept confidential according to EEO guidelines.

Artech logo

About Artech

Sourced by ZipRecruiter

Artech is a leading IT staffing and consulting company based in Morristown, NJ, US. Since its foundation in 1992, Artech has mastered in complementing human expertise with technology and business acumen to produce world-class staffing solutions. The company caters to diverse industry sectors, including financial services, healthcare, telecommunication, energy and utilities, supply chain, and retail. It provides IT consulting, project management, professional and staff augmentation, and managed staffing services. Artech's mission is to provide exceptional IT staffing services to its clients by comprehending their business needs and then crafting a customized staffing strategy. Its notable achievement includes being recognized as one of the largest IT staffing companies in the U.S, according to Staffing Industry Analysts (SIA).

Industry

Recruiting and staffing services

Company size

10,000+ Employees

Headquarters location

Morristown, NJ, US

Year founded

1992

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