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Research Associate Jobs in New Jersey (NOW HIRING)

IBR is currently seeking a Research Associate . This position is in-person, in Hamilton, NJ. Responsibilities: * Design and validate microbiological and molecular diagnostic assays. * Design and ...

Position Details Position Information Recruitment/Posting Title Research Associate II Job Category Staff & Executive - Healthcare Department NJMS - Pharmacology Overview New Jersey's academic health ...

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Position Details Position Information Recruitment/Posting Title Research Associate II Job Category Staff & Executive - Healthcare Department NJMS - Pharmacology Overview New Jersey's academic health ...

Though we faced many challenges, we remained fearless in our research and rigorous in our thinking, pushing ourselves to work harder. However, what affected us the most was the enormous burden ...

Though we faced many challenges, we remained fearless in our research and rigorous in our thinking, pushing ourselves to work harder. However, what affected us the most was the enormous burden ...

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Research Associate information

See New Jersey salary details

$16

$33

$47

How much do research associate jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for research associate in New Jersey is $33.04, according to ZipRecruiter salary data. Most workers in this role earn between $26.59 and $37.60 per hour, depending on experience, location, and employer.

What is a research associate?

Research Associates are professionals who support research projects in academic, scientific, or business settings. They assist with designing studies, collecting and analyzing data, and preparing reports or publications. Research Associates often work under the supervision of principal investigators or senior researchers, contributing their expertise to advance the goals of the project. Their responsibilities can vary depending on the field, but typically involve both administrative and hands-on research tasks.

What does a research associate do?

As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.

What are the key skills and qualifications needed to thrive as a research associate, and why are they important?

To thrive as a Research Associate, you need a strong background in research methodology, data analysis, and subject-specific knowledge, typically supported by a relevant bachelor's or master's degree. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, and research databases is often essential. Attention to detail, critical thinking, and clear written and verbal communication skills set outstanding Research Associates apart. These skills ensure accurate data collection, effective collaboration, and the production of reliable, impactful research outcomes.

What are some typical challenges a research associate might face when managing multiple research projects simultaneously?

As a Research Associate, juggling multiple projects often requires strong organizational skills and the ability to prioritize tasks effectively. You might encounter challenges such as balancing deadlines, coordinating with various team members, and adapting to shifting project goals or data requirements. Effective communication and proactive time management are essential to ensure each project progresses smoothly and meets its milestones. Many teams use project management tools and regular check-ins to help mitigate these challenges and support collaboration.

What is the difference between Research Associate vs Research Scientist?

AspectResearch AssociateResearch Scientist
Required CredentialsBachelor's or Master's degree in relevant fieldMaster's or PhD in relevant field
Work EnvironmentLaboratories, research institutions, universitiesLaboratories, research institutions, industry settings
Employer & Industry UsageAcademic, government, non-profitAcademic, industry, biotech, pharma
Common Search & ComparisonYesYes

The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.

What qualifications do you need to be a research associate?

Research associates typically need a bachelor's degree in a relevant field such as science, engineering, or social sciences. Many positions prefer or require a master's degree or higher, along with strong analytical skills, proficiency with research tools, and experience in data collection and analysis.

What are the most commonly searched types of Research jobs in New Jersey?

The most popular types of Research jobs in New Jersey are:

What are popular job titles related to Research Associate jobs in New Jersey?

For Research Associate jobs in New Jersey, the most frequently searched job titles are:

What job categories do people searching Research Associate jobs in New Jersey look for?

The top searched job categories for Research Associate jobs in New Jersey are:

What cities in New Jersey are hiring for Research Associate jobs?

Cities in New Jersey with the most Research Associate job openings:

Infographic showing various Research Associate job openings in New Jersey as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $68,717 per year, or $33 per hour.

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


CentraState Healthcare System rating

5.9

Company rating: 5.9 out of 10

Based on 15 frontline employees who took The Breakroom Quiz


Job description

Overview

CentraState Healthcare System, headquartered in Freehold, New Jersey, is a leading nonprofit healthcare provider dedicated to serving the community. Its comprehensive network includes CentraState Medical Center, a community-focused hospital, along with an ambulatory campus, two senior living facilities, three free-standing community health pavilions, and a charitable foundation. As the third-largest employer in Monmouth County, CentraState has earned repeated recognition as a Great Place to Work-Certified company, reinforcing its reputation as an exceptional workplace. 

CentraState has an employment opportunity available for a Research Associate. This role administers professional research standards in accordance with hospital policies and in alignment with the guidelines of the National Institutes of Health and the U.S. Food and Drug Administration (FDA). The Research Associate ensures patient safety and protection while maintaining a high level of clinical research quality.

Responsibilities
  • Responsible for all IRB processes (local, central or partner facility).
  • Participates in site feasibility and protocol activation meetings.
  • Ascertains that there is documented Institutional Review Board (IRB) approval for protocols prior to activation meeting.
  • Actively participates in selection of appropriate patients for study in collaboration with physician.
  • Administers patient evaluation and assessment tests as appropriate.
  • Completes the pre-study work including preparation of internal study binder, source document development and case report form development if necessary.
  • Develops the calendar for the protocol.
  • Participates in protocol activation meetings.
  • Ascertains that pretreatment and eligibility of the protocol have been met including a completed informed consent obtained prior to registration. Responsible for the patient receiving a signed copy of the consent form.
  • Abstracts data from various sources to retrieve the necessary information to complete eligibility checklists, pre-study flow sheets, pathology reports, etc to confirm patient eligibility.
  • Review pre-study information to confirm eligibility and register the patient.
  • Documents the patient registration in the database. Places patient name and calendar in the internal study binder.
  • Reviews protocol enrollment forms for patients entered onto trials by affiliate investigators, reviews copies of eligibility test results provided by affiliate investigators, and confirms eligibility prior to protocol initiation.
  • Reinforces explanations of clinical trials to patients, significant others and personnel.
  • Assists in the reporting of adverse events and completion of required forms.
  • Maintains current knowledge of protocols, eligibility requirements, and amendments.
  • Completes pharmaceutical company Case Report Forms and cooperative group flow sheets.
  • Maintains active and follow up list of patients.
  • Obtains data from outside sources (physician offices/hospitals) as needed for data collection and submission.
  • Obtains all data information from affiliate centers. Ensures that they are following the protocols correctly. Provides them with a calendar to follow.
  • Maintains, updates records on protocol patients.
  • Prepares a follow-up calendar for the appropriate protocols.
  • Obtains and submits x-rays, operative/pathology report, or other specialized reports as needed.
  • Submits pathology or other lab materials and appropriate forms when required.
  • Notifies the appropriate physician, staff, and the Director of Pharmacy of all serious adverse events (SAE). Compiles all necessary forms related to SAE's.
  • Completes and submits all follow-up forms for cooperative groups and pharmaceutical clinical trials.
  • Acts as a resource to all personnel to assist in maintaining protocol compliance re study calendar dose modifications, etc.
  • Maintains all protocol related items organized, including patient charts, shadow charts and Case Report Forms.
  • Participates in all necessary meetings required for the specific tumor study group.
  • Acts as liaison with sponsor organization and pharmaceutical companies coordinating research studies.
  • Attends and participates in clinical research meetings.
  • Evaluates protocol study forms for completeness, accuracy and compliance to protocol.
  • Complete Quality Assurance form for calendars, eligibility checklists and source documents.
  • Review records and forms prior to an audit.
  • Gather records, reports, radiographs, scans and other necessary materials required at the time of site visits by cooperative groups, pharmaceutical companies, or the FDA.
  • Communicates effectively with staff and others.
  • Anticipates and responds to the needs of others, providing assistance in a courteous quick manner.
  • Assists in the promotion of team work.
  • Responds appropriately to incoming communications.
  • Consistently abides by the Food and Drug Administration (FDA) and IRB policies and procedures.
Qualifications
  • Bachelor's degree in related healthcare field required.
  • Previous experience in clinical research preferred.
  • Research Certification through Association of Clinical Research Professionals or Society of Clinical Research Professionals preferred or obtained within 6 months of hire
  • Strong professional, organizational, and interpersonal skills to effectively relate with all members of the healthcare team.
About Us

CentraState Healthcare System, in partnership with Atlantic Health System, is a fully accredited, not-for-profit, community-based health system dedicated to providing comprehensive health services in central New Jersey. Beyond offering a wide range of advanced diagnostic and treatment options, CentraState is committed to being a valuable health partner, focusing on disease prevention, promoting healthy behaviors, and helping individuals of all ages live well.

Located in Freehold, CentraState includes a 284-bed acute-care hospital, a dynamic health and wellness campus, two award-winning senior living communities, a charitable foundation, and convenient satellite health pavilions. These pavilions offer primary care, specialty physician practices, and access to outpatient services such as lab work and physical therapy.

CentraState is proud to be among the less than two percent of hospitals nationwide to earn Magnet designation for nursing excellence five times. Additionally, it has been recognized as a Great Place to Work-Certified Company by Great Place to Work for four consecutive years.

Joining CentraState means becoming part of a pioneering healthcare facility committed to high-quality, patient-focused care. We invite you to make a difference in our community and advance your career with us. We support our employees with work/life balance initiatives, tuition assistance, career advancement opportunities, and more.

Discover why our employees love their jobs and being part of the CentraState family!

CentraState Health System offers a competitive and comprehensive Total Rewards package that supports the health, financial security, and well-being of all team members.

What We Offer:

  • Medical, Dental, Vision, Prescription Coverage (30 hours per week or above for full-time and part-time team members)
  • Life & AD&D Insurance
  • Long-Term Disability (with options to supplement)
  • 403(b) Retirement Plan with employer match
  • 401(a) Retirement Plan with employer contribution
  • PTO
  • Tuition Reimbursement
  • Well-Being Rewards
  • Employee Assistance Program (EAP)
  • Fertility Coverage, Healthy Pregnancy Program
  • Flexible Spending & Commuter Accounts
  • Pet, Home & Auto, Identity Theft and Legal Insurance
  • Growth Opportunity and Workforce Development Initiatives
  • Continuing Education / Onsite Training
  • A warm, welcoming company culture based upon mutual respect and a collaborative goal of providing excellent patient care
  • Concierge Services with Work & Family Benefits
  • Magnet recognized healthcare facility

 

Compensation Range: $35.00 - $59.50 per hour

 

The compensation above reflects the established range from CentraState Healthcare System (CSHS) for this position at the time the job was posted. CSHS considers many factors to determine compensation, including education, experience, skills, licenses, certification, and training.  As such, team member compensation may fall outside this range. 

Additionally, the compensation range reflects base salary and does not include extra shift rates or incentives tied to quality, productivity, etc., as applicable.

The benefits outlined also reflect CSHS' policy at the time of posting.  Benefits as are made available to other similarly situated team members of CSHS, although participation is at all times in accordance with and subject to the eligibility and other provisions of such plans and programs. CSHS may modify its benefits plans or programs at any time.

CSHS is proud to comply with all pay equity and pay transparency laws.

Employment Type: FULL_TIME

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