ZipRecruiter

Log In

1

Study Monitor Jobs in New York (NOW HIRING)

next page

Showing results 1-20

All JobsStudy Monitor JobsStudy Monitor Jobs in New York

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 Jul 29, 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 does a study monitor do?

A study monitor oversees clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. They review data for accuracy, verify patient safety, and ensure proper documentation throughout the trial process. Monitoring often involves site visits, reporting, and collaboration with research teams.

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

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 jobs pay $500,000 a year in the US?

High-paying roles for study monitors are rare, as most positions in this field typically do not reach $500,000 annually. However, top executives or specialists in clinical research or pharmaceutical industries can earn such salaries through bonuses, stock options, or profit sharing. Achieving this level often requires extensive experience, advanced degrees, and leadership responsibilities.

How to become a study monitor?

To become a study monitor, candidates typically need to be responsible students with good academic standing and strong communication skills. Some positions require a minimum age or grade level, and previous experience or recommendations may be helpful. Often, applications involve submitting a form or resume and may include an interview or training before starting the role.

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.

What is a Study Monitor job?

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 degree do I need to be a clinical research coordinator?

A clinical research coordinator typically needs at least a bachelor's degree in a health-related field such as biology, nursing, or healthcare administration. Some positions may require or prefer a master's degree or relevant certifications like the Certified Clinical Research Professional (CCRP). Experience with clinical trials and knowledge of Good Clinical Practice (GCP) guidelines are also important.
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 July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 1% Temporary, and 4% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $84,528 per year, or $40.6 per hour.

Clinical Study Director

Artech Information System LLC

Bridgewater, NJ • On-site

Contractor

Re-posted 4 days ago

Job description

Company Description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual 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 and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

This role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science & Operations Platform (CSO) of Sanofi R&D. The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility, ...) performed by the CSO. The CSD will provide appropriate medical input and support for all these clinical activities. He/she will provide medical training and medical information to study team(s), Clinical Study Units (CSUs) and investigators. He/she will be deeply involved in the feasibility process. He/she will be accountable for medical review and will collaborate and interact with Pharmacovigilance to review safety data. He/she will interact with Medical Advisors in CRUs or Disease Units), a specialization in a medical area would be requested or at least appreciated.

Scope:


All clinical studies related to projects in clinical development (excluding Clinical & Exploratory Pharmacology studies) and medical investigations (e.g. Registry, survey) for projects in development or for marketed drugs.


Key Individual Accountabilities:

Medical reference and medical expertise for operational strategy within the CSO for study registries he/she is allocated to

Medical consultant for projects to be proposed to the CSO

Medical contact for interaction with physicians responsible for the project or the study at the customer level

Support with his/her medical knowledge and background a study or a project from

business negotiation with customers to final product delivery (e.g. study completion or

project report or publication)

Conduct the feasibility for study/project with the feasibility manager and other team members (especially Medical Advisors in CSUs)

Prepare and/or organize and/or participate to Investigator's Meetings, Steering Committees, Data Monitoring Committee meetings (only "open" part of the DMC meetings).

Prepare and/or approve any documents related to the study and requiring a medical expertise (extended synopsis, protocol, medical training material for study monitoring team and for investigators)

Provide medical training to study team, CSUs (Medical Advisors, monitoring) and investigators

Develop interaction with Medical Advisors in CSUs for the best knowledge of the study, compound protocol

Participate to Investigators meetings

Provide medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts

Participate to clinical trial team (and cluster if any) meetings

Accountable for the medical review of data done by the clinical trial team, the case by case review of safety events reported to GPE and coding of events and drugs

Provide appropriate medical input for patient recruitment and retention strategy

Support the CSUs and affiliates to develop network of KOLs and experts and to select National Coordinators or members of Study Committees

Prepare and provide key medical information to investigators and/experts in respect with communication policies (e.g. study results, DMC advice)


Qualifications

Basic Qualifications:

Licensed United States Medical Doctor or an International medical graduate who has certification by the Educational Commission for Foreign Medical Graduates (ECFMG).     

2-3 or more years of Phase 2/3 Clinical Research / Drug Development experience in the pharmaceutical industry. 


Preferred Qualifications:

Knowledge in ICH, GCP and local regulations

Fluent in English (writing and speaking)

Additional Clinical Research and/or Drug Development experience in other therapeutic areas, especially Immunology. 


Additional Information


Sneha Shrivastava

Technical Recruiter (Clinical/Scientific)

 Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 

Office: 973.967.3348 | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | Twitter



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

View All Artech Jobs

Apply