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Study Monitor Jobs in New York (NOW HIRING)

US Tech Solutions

Senior Study Manager

Jersey City, NJ · On-site

CRO selection, CRF development, drug forecasting, study manuals, monitoring plan, data management plan, definition of end points, selection of safety and efficacy assessments, recruitment planning ...

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Study Monitor information

See New York salary details

$18.6K

$84.5K

$150.9K

How much do study monitor jobs pay per year?

As of Aug 19, 2026, the average yearly pay for study monitor in New York is $84,528.00, according to ZipRecruiter salary data. Most workers in this role earn between $48,103.00 and $124,632.00 per year, depending on experience, location, and employer.

What is a study monitor?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

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

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges study monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

How do you become a study monitor?

To become a study monitor, candidates typically need to be students with good academic standing and demonstrate responsibility. The process often involves applying through the school or organization, sometimes including an interview or recommendation, and may require training on supervision and safety protocols.

What are popular job titles related to Study Monitor jobs in New York?

For Study Monitor jobs in New York, the most frequently searched job titles are:

What job categories do people searching Study Monitor jobs in New York look for?

The top searched job categories for Study Monitor jobs in New York are:

Study Monitor jobs near you
Infographic showing various Study Monitor job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $84,528 per year, or $40.6 per hour.

Study Coordinator

Albert Einstein College of Medicine

Bronx, NY

$58K/yr

Full-time

Posted 7 days ago

Job description

POSITION RESPONSIBILITIES
    • Support the planning, coordination, and monitoring of multicenter project implementation
     
    • Provide training and education on informatics tools within the ICU setting
     
    • Travel as needed to conduct site visits and deliver project-related training
     
    • Collect, manage, and accurately document research data and outcomes
     
    • Oversee study implementation at Montefiore and collaborating sites
     
    • Collaborate with research coordinators to ensure adequate study coverage
     
    • Lead patient screening and recruitment efforts
     
    • Perform data entry and maintain data integrity for ongoing projects
     
    • Ensure adherence to research protocols and study guidelines
     
    • Maintain organized and compliant clinical research records
     
    • Foster effective communication with clinical, professional, and ancillary staff
     
    • Assist with Institutional Review Board (IRB) submissions and regulatory documentation
     
    • Perform additional related duties as assigned
QUALIFICATIONS
  • Bachelor's Degree required.
  • Experience in medical or public health research is preferred.
  • Ability to manage multiple priorities and projects while working as part of a team.
  • Strong computer skills, including MS Excel.
  • Clinical Research experience preferred
  • Bilingual (Spanish) preferred
Salary VerbiageIn compliance with NYC's Pay Transparency Act, the annual base salary range for this position is listed below. Albert Einstein College of Medicine considers factors such as (but not limited to) scope and responsibilities of the position, candidate's work experience, education/training, key skills, internal peer equity, as well as, market and organizational considerations when extending an offer.Minimum Salary RangeUSD $58,500.00/Yr.Maximum Salary RangeUSD $58,500.00/Yr.ABOUT US

Position

The Critical Care Study Coordinator will have responsibilities to support and assist the MD in administering and monitoring and daily operation of all critical care research projects. This position will be fully involved in all critical care studies and clinical trials, and will responsible for educating and training ICU staff on the division's studies, protocol and importance; manage mechanisms for identifying eligible patients and their surrogates; manage subject interviews; initiate, manage, and coordinate several observational research studies and clinical trials in sepsis, acute lung injury and other critical illnesses. The position will also oversee subject recruitment, interviews, sample collection and processing, training of research and clinical staff, monitoring/reporting of research compliance and adverse events, data collection and entry, FDA and multicenter paperwork/interactions and other duties. Additional observational and/or therapeutic protocols are likely. SC must be willing to be flexible with the hours as needed for the study.

Employment Type: OTHER

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