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Part Time Clinical Research Associate Jobs in New York

New York University

Research Associate

New York, NY · On-site

$26.37/hr

Description PART-TIME RESEARCH ASSOCIATE New York University Tandon School of Engineering The Department of Computer Science and Engineering at NYU Tandon School of Engineering is seeking to hire a ...

New York University

Research Associate

New York, NY · On-site

$26.37/hr

Description PART TIME RESEARCH ASSOCIATE New York University Tandon School of Engineering CUSP UO (Urban Observatory) at NYU Tandon School of Engineering is seeking to hire a Part Time Research ...

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Part Time Clinical Research Associate information

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How much do part time clinical research associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for part time clinical research associate in New York is $44.99, according to ZipRecruiter salary data. Most workers in this role earn between $31.54 and $57.60 per hour, depending on experience, location, and employer.

What is a part time clinical research associate?

Part-time Clinical Research Associates (CRAs) are professionals who monitor and manage clinical trials on a flexible or reduced-hour schedule, rather than full-time. They are responsible for ensuring that studies comply with regulatory requirements, collecting data, and acting as a liaison between clinical trial sites and sponsors. Part-time CRAs may work remotely or travel to research sites as needed, and their schedules can vary depending on the needs of the research project. This role is ideal for those seeking work-life balance or supplementing other professional activities. Their work is critical in advancing medical research and ensuring patient safety.

What are the key skills and qualifications needed to thrive as a part time clinical research associate?

To thrive as a Part Time Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical research protocols, and often a bachelor’s degree in a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certification such as ACRP or SOCRA is highly valued. Strong attention to detail, organizational skills, and effective communication are essential soft skills for monitoring trials and collaborating with research teams. These skills ensure regulatory compliance, accurate data collection, and efficient trial execution, all critical for successful clinical research outcomes.

What are some common challenges faced by part time clinical research associates, and how can they be managed effectively?

Part-time Clinical Research Associates (CRAs) often face the challenge of balancing multiple study sites and projects within limited working hours. Time management and clear communication with both the research team and site staff are crucial to ensure all monitoring visits, documentation, and regulatory requirements are met on schedule. Additionally, part-time CRAs may need to be proactive in staying updated on study protocols and industry regulations, as they may not be present for all in-person team meetings. Establishing structured routines and leveraging digital tools for remote collaboration can help manage these challenges effectively.

What is the difference between Part Time Clinical Research Associate vs Clinical Research Coordinator?

AspectPart Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often certifications like CCRP or RACBachelor's degree, often certifications like CCRP or RAC
Work EnvironmentMonitoring clinical trials at sites, remote or onsiteManaging trial operations at research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinics
Search & Comparison IntentUnderstanding monitoring roles in trialsManaging trial activities at sites

Part Time Clinical Research Associates primarily focus on monitoring clinical trial progress, ensuring compliance, and verifying data accuracy, often working remotely or onsite. Clinical Research Coordinators handle the day-to-day operations at research sites, including patient recruitment and data collection. Both roles require similar credentials but differ in responsibilities and work settings.

What are the most commonly searched types of Part Time Clinical Research jobs in New York?

The most popular types of Part Time Clinical Research jobs in New York are:

What are popular job titles related to Part Time Clinical Research Associate jobs in New York?

For Part Time Clinical Research Associate jobs in New York, the most frequently searched job titles are:

What job categories do people searching Part Time Clinical Research Associate jobs in New York look for?

The top searched job categories for Part Time Clinical Research Associate jobs in New York are:

What cities in New York are hiring for Part Time Clinical Research Associate jobs?

Cities in New York with the most Part Time Clinical Research Associate job openings:

Part Time Clinical Research Associate jobs near you
Infographic showing various Part Time Clinical Research Associate job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $93,586 per year, or $45 per hour.

Clinical Research Associate - Part Time

Saint Peter's Healthcare System

New Brunswick, NJ • On-site

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement

Re-posted 13 hours ago

Saint Peter's University Hospital rating

8.0

Company rating: 8.0 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

137th of 1,065 rated hospitals

Job description

Clinical Research Associate - Part Time
MFM Clinical Study Grant
The Clinical Research Associate - Part Time will:
  • Serve as the organizational appointee for assigned MFM research projects, maintaining the relationship and oversight of study procedures.
  • Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and updating the Informed Consent Form with CIRB Boilerplate, Completion of Institutional Review Board (IRB) modifications with supporting documentation.
  • Maintain oversight of designated research project study activities including performing the following functions: Subject recruitment, Consenting and Enrollment/Randomization, Perform study procedures/assessments in accordance with clinical trial guidelines, Complete Data Entry into Case Report Forms and Query Resolution, Process/Ship Specimens per trial requirements, Maintain Regulatory files including delegation logs, FDA form 1572, training logs and other trial documents in compliance with federal and local regulations, Process IRB amendments, annual renewals, closures, etc, Attend regular meetings with members of the project at partnering institutions and sponsors to report on study progress.
  • Maintain financial records including Accounts Receivable Report, Check remittance with back-up details and assist with the annual A-133 audit.
  • Serve as a liaison between investigators, research staff, hospital staff, the IRB and sponsors.
  • Maintain and utilize research's Clinical Trial Management System (CTMS).
  • Maintain strict patient confidentiality including restricted access to clinical trial files.
  • Attend and participate in research meetings and report on study progress.
  • Perform other tasks as assigned by leadership.
  • Comply with all SPUH policies, procedures, objectives, quality assurance, safety, environmental and infection controls.

Requirements:
  • Bachelor's Degree in science or healthcare field preferred.
  • Two years of experience in healthcare and/or research.
  • Ability to work independently as well as in a team environment.
  • Proficient in Microsoft Office Suite.
  • Certified Clinical Research Professional (CCRP) or other similar research accreditation preferred.
  • Previous Phlebotomy experience or certification preferred.

Salary Range: 24.33 - 38.93 USD
We offer competitive base rates that are determined by many factors, including job-related work experience, internal equity, and industry-specific market data. In addition to base salary, some positions may be eligible for clinical certification pay and shift differentials.
The salary range listed for exempt positions reflects full-time compensation and will be prorated based on employment status.
Saint Peter's offers a robust benefits program to eligible employees that will support you and your family in working toward achieving and maintaining secure, healthy lives now and into the future. Benefits include medical, dental, and vision insurance; savings accounts, voluntary benefits, wellness programs and discounts, paid life insurance, generous 401(k) match, adoption assistance, back-up daycare, free onsite parking, and recognition rewards.
You can take your career to the next level by participating in either a fully paid tuition program or our generous tuition assistance program. Learn more about our benefits by visiting our site at Saint Peter's.

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