ZipRecruiter

Log In

1

Study Monitor Jobs in New York (NOW HIRING)

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

System One

Director Medical Monitor

Parsippany, NJ · On-site

Director Medical Monitor Location: Parsippany, NJ Type: Direct Hire Contractor Work Model: Hybrid ... Provide medical oversight for assigned clinical studies from study start-up through closeout.

Barrington James

Nurse Practitioner

Manhattan, NY · On-site

Collaborate with Sponsors, Study Monitors, and Medical Monitors * Complete required sponsor training and attend investigator meetings as needed * Maintain accurate and timely clinical documentation ...

Icon plc

Clinical Study Lead

Warren, NJ · Hybrid

$121K - $151K/yr

Clinical Study Lead ICON is a global healthcare intelligence and clinical research organisation ... Performs timely review of monitoring reports from CRO and associated deliverables demonstrating ...

previous page

Showing results 41-60

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 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.

Sr. Clinical Trial Study Manager - Oncology

Syndicus, Inc

Parsippany, NJ • On-site

Full-time

Re-posted 15 days ago

Job description

Company Description
Job Description
Sr. Clinical Trial Study Manager - Oncology
Whippany, NJ
Sr. Study Manager Job description
The incumbent will:
• Manages and is responsible for all activities related to clinical pharmacology, complex phase I, extended phase
I/IIa oncology clinical trials from the approved study concept to the clinical study report.
• Manages all Study Team activities as defined per SOPs/OIs and ensures the organization of
regular Study Team meetings
• Manages the selection and oversight of External Suppliers (e.g. site management and
monitoring CROs, Central Labs, central ECG reading center, etc.)
• Develops and manages budget, timelines and quality of the study and its deliverables.
Responsible for forecasting and tracking of study costs. Ensuring all relevant IT-systems are
updated with current and accurate information (e.g. IMPACT)
• Responsible for all start up activities e.g. 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 and oversight.
• Writes protocols and amendments in collaboration with study team members
• Responsible for study specific feasibility and site selection to meet study enrollment and
timelines.
• Together with OPL and ECL/CPL responsible for developing the total external study budget
and accountable for providing monthly and yearly estimates, tracking study budget, initiating
payments, providing monthly information to controlling, OPL, ECL/CPL, identifying
budget/estimate issues and proactively developing a plan for resolving study finance issues.
• Tracks and compiles patient enrollment, data quality and cleaning progress and overall study
progress and ensures study timelines are met
• Responsible for training and oversight of CROs to ensure compliance with timelines and
budget.
• Develops appropriate study related training for monitors and site personnel according to GCP
and company standards
Qualifications
Qualifications
The qualified candidate is required to possess the following:
• Bachelor's degree or equivalent education with 8+ years of relevant healthcare experience of which 5 years working in early clinical operations pharmaceutical (preferably oncology) including direct monitoring and clinical trial/study management experience.
Ideal candidate will have solid clinical operations experience working as a study manager including 2 years of monitoring experience and a minimum of 3 years of study management (early oncology) experience is preferred
• The incumbent is responsible for the direct management of Phase I & IIa complex oncology global clinical trials. This requires an in-depth knowledge of study management/project management. In addition Good Clinical Practices (GCP), federal regulations and international regulations (International Harmonization Committee-ICH regulations).
The position also requires strong awareness and understanding of cultural differences as well as regional operational differences.
• Demonstrated leadership in project management and vendor management.
• The incumbent requires comprehensive knowledge of the drug development process including, monitoring, regulatory requirements, drug safety requirements, data management processes and budget parameters.
• Effective written and verbal communication, thorough knowledge of oral and written English, strong oral presentation, and excellent interpersonal, decision-making and issue resolution skills are required. In addition, the incumbent requires effective planning and organization skills, attention to detail and excellent follow through.
Additional Information
All your information will be kept confidential according to EEO guidelines.

Apply