Research Manager Jobs in New Jersey
Research Manager jobs in New Jersey are in strong demand, concentrated in pharmaceuticals, biotechnology, clinical research, and consumer insights, with openings at every level from junior research associate to senior director. The most active hiring metros are Princeton, Parsippany, and Newark, where companies like Johnson & Johnson, Merck, and Bristol Myers Squibb maintain major research operations. The most sought-after specialties in New Jersey are clinical research management, market research, and scientific research program oversight. Find a role that fits below and apply directly.
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Showing 5 of 14+ Research Manager jobs
Company Overview
Cardio Metabolic Institute is a multifaceted practice focused on cardiovascular and metabolic problems.
Overview
We are seeking a Clinical Research Site Manager to lead the daily operations of our investigator research site and clinical trial portfolio, from feasibility and study startup through closeout. You will supervise research staff, serve as the site’s operational liaison to Principal Investigators, sponsors, and CROs, and conduct participant study visits as trained and delegated. Your impact: careful oversight of study conduct and participant safety helps protect participants and supports reliable research findings. Medical decisions and investigator responsibilities remain with the qualified investigators.
Responsibilities
· Manage clinical trials and research projects, coordinating timelines, study activities, visit coverage, and team responsibilities across active and upcoming studies.
· Lead feasibility and study activation, including protocol review, visit workflows, source templates, system access, training, supplies, and coordination with laboratories, pharmacies, and other service providers.
· Conduct participant study visits as trained and delegated, including coordination of blood sampling and clinical laboratory activities as applicable, while keeping sufficient time for management duties.
· Recruit, onboard, supervise, and coach clinical research coordinators, research assistants, and other site staff; hold monthly team meetings and document training and action items.
· Oversee data collection and data management; review study documentation for completeness, accuracy, and compliance, and ensure queries are resolved on time.
· Monitor participant safety and study progress; ensure eligibility decisions, consent activities, safety concerns, and protocol deviations reach qualified personnel promptly.
· Oversee participant recruitment, retention, referral coordination, and scheduling.
· Apply Food and Drug Administration (FDA) regulations, International Council for Harmonisation (ICH) guidelines, Good Clinical Practice (GCP), and ethical and healthcare compliance requirements; maintain inspection readiness and coordinate monitoring visits, audits, and corrective and preventive actions.
· Support clinical quality assurance, compliance management, and use of electronic medical record (EMR) systems, clinical trial management and electronic data capture systems, and statistical software.
· Partner with budget, contracting, and billing staff so that performed visits and procedures are captured accurately and expenses stay within approved budgets.
· Serve as the site’s operational contact for investigators, sponsors, CROs, monitors, and vendors, and maintain SOPs that improve workflows and reduce repeat errors.
Requirements
· Bachelor’s degree in health, life science, nursing, public health, or a related field, or equivalent education and experience.
· At least five years of clinical research experience, including two years of staff supervision or research team leadership; experience managing multiple interventional studies at an investigator site, from startup through closeout.
· Working knowledge of FDA requirements, ICH GCP, human-subject protections, HIPAA, and IRB processes; practical knowledge of GCP and clinical ethical guidelines is expected.
· Knowledge of medical terminology, clinical research methods, research project management, documentation review, and compliance.
· Proficiency with CTMS, EDC, electronic source and regulatory systems, and Microsoft Office (especially Excel); familiarity with CDISC standards, data management, patient monitoring, and clinical laboratory practices.
· Ability to manage competing priorities, address performance concerns, identify quality risks, and communicate effectively with investigators, staff, and external partners.
Preferred Qualifications
· ICH GCP certificate from any valid issuer; ACRP CCRC or ACRP-CP, or SOCRA CCRP certification.
· Experience with sponsor budgets, research billing, and quality improvement, and in the site’s therapeutic areas. An RN license is preferred only when relevant to assigned duties.
Schedule
Full time and onsite, with occasional early, late, or weekend coverage and local travel as study needs require.
Pay: $64,300.00 - $77,500.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Retirement plan
- Vision insurance
Work Location: In person
Company Overview
Cardio Metabolic Institute is a multifaceted practice focused on cardiovascular and metabolic problems.
Overview
We are seeking a Clinical Research Site Manager to lead the daily operations of our investigator research site and clinical trial portfolio, from feasibility and study startup through closeout. You will supervise research staff, serve as the site’s operational liaison to Principal Investigators, sponsors, and CROs, and conduct participant study visits as trained and delegated. Your impact: careful oversight of study conduct and participant safety helps protect participants and supports reliable research findings. Medical decisions and investigator responsibilities remain with the qualified investigators.
Responsibilities
· Manage clinical trials and research projects, coordinating timelines, study activities, visit coverage, and team responsibilities across active and upcoming studies.
· Lead feasibility and study activation, including protocol review, visit workflows, source templates, system access, training, supplies, and coordination with laboratories, pharmacies, and other service providers.
· Conduct participant study visits as trained and delegated, including coordination of blood sampling and clinical laboratory activities as applicable, while keeping sufficient time for management duties.
· Recruit, onboard, supervise, and coach clinical research coordinators, research assistants, and other site staff; hold monthly team meetings and document training and action items.
· Oversee data collection and data management; review study documentation for completeness, accuracy, and compliance, and ensure queries are resolved on time.
· Monitor participant safety and study progress; ensure eligibility decisions, consent activities, safety concerns, and protocol deviations reach qualified personnel promptly.
· Oversee participant recruitment, retention, referral coordination, and scheduling.
· Apply Food and Drug Administration (FDA) regulations, International Council for Harmonisation (ICH) guidelines, Good Clinical Practice (GCP), and ethical and healthcare compliance requirements; maintain inspection readiness and coordinate monitoring visits, audits, and corrective and preventive actions.
· Support clinical quality assurance, compliance management, and use of electronic medical record (EMR) systems, clinical trial management and electronic data capture systems, and statistical software.
· Partner with budget, contracting, and billing staff so that performed visits and procedures are captured accurately and expenses stay within approved budgets.
· Serve as the site’s operational contact for investigators, sponsors, CROs, monitors, and vendors, and maintain SOPs that improve workflows and reduce repeat errors.
Requirements
· Bachelor’s degree in health, life science, nursing, public health, or a related field, or equivalent education and experience.
· At least five years of clinical research experience, including two years of staff supervision or research team leadership; experience managing multiple interventional studies at an investigator site, from startup through closeout.
· Working knowledge of FDA requirements, ICH GCP, human-subject protections, HIPAA, and IRB processes; practical knowledge of GCP and clinical ethical guidelines is expected.
· Knowledge of medical terminology, clinical research methods, research project management, documentation review, and compliance.
· Proficiency with CTMS, EDC, electronic source and regulatory systems, and Microsoft Office (especially Excel); familiarity with CDISC standards, data management, patient monitoring, and clinical laboratory practices.
· Ability to manage competing priorities, address performance concerns, identify quality risks, and communicate effectively with investigators, staff, and external partners.
Preferred Qualifications
· ICH GCP certificate from any valid issuer; ACRP CCRC or ACRP-CP, or SOCRA CCRP certification.
· Experience with sponsor budgets, research billing, and quality improvement, and in the site’s therapeutic areas. An RN license is preferred only when relevant to assigned duties.
Schedule
Full time and onsite, with occasional early, late, or weekend coverage and local travel as study needs require.
Pay: $64,300.00 - $77,500.00 per year
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Retirement plan
- Vision insurance
Work Location: In person
See All 14 Research Manager Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Research Manager JobsResearch Manager Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Research Manager Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Education
What New Jersey Employers Look For
The qualifications that appear most often in research manager jobs across New Jersey.
- Bachelor's or master's degree in a scientific, social science, or business field required
- Minimum three to five years of experience managing research projects or teams
- Proficiency with research methodologies including quantitative and qualitative analysis
- Experience with clinical trial or product development lifecycles in regulated industries
- Strong project management skills, including budget oversight and stakeholder communication
- Familiarity with IRB processes, GCP guidelines, or FDA regulatory requirements preferred
Research Manager Jobs in New Jersey: Frequently Asked Questions
How do you become a research manager in New Jersey?
Most research manager positions in New Jersey require a bachelor's degree at minimum, with a master's degree strongly preferred in scientific or clinical fields. There is no single state-issued license for research managers, but candidates targeting clinical research roles benefit from earning a Certified Clinical Research Professional credential through the Society of Clinical Research Associates. New Jersey's dense pharmaceutical and biotech corridor means employers in that sector routinely expect familiarity with FDA regulations and Good Clinical Practice guidelines alongside formal education.
How much do research managers make in New Jersey?
Research managers in New Jersey earn a median of about $207,030 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $136,840 for the lowest 10% to over $317,420 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire research managers in New Jersey?
Employers hiring research managers in New Jersey right now include Atlantic Health, Rutgers University, and ETS, based on current listings on Migrate Mate as of November 2026. New Jersey's pharmaceutical and life sciences concentration means a large share of these openings come from multinational research organizations with long-standing operations in the state.
Which New Jersey cities have the most research manager jobs?
The cities with the most research manager openings in New Jersey are Princeton, Morristown, and New Brunswick. That distribution reflects the state's pharmaceutical corridor anchored around Princeton and Parsippany, where major life sciences headquarters cluster, and Newark's broader corporate and academic research base, which supports consumer insights, public health, and technology-driven research roles.
Are there remote research manager jobs in New Jersey?
Yes, and more than many comparable roles, since research management work is largely analytical, project-based, and communication-driven rather than tied to a physical lab or facility. About 50% of research manager openings tied to New Jersey are remote or hybrid as of November 2026, reflecting real flexibility in the market. The functions most commonly offered remotely include market research management, competitive intelligence oversight, and research program coordination roles outside of regulated clinical or laboratory settings.
How can I get hired as a research manager in New Jersey with little or no experience?
The most realistic entry path is moving into a research coordinator or research associate role first, which large New Jersey employers in pharma and biotech regularly hire at the new-graduate level. Companies like Johnson & Johnson and Merck run rotational or early-career development programs in their New Jersey operations that place candidates on research project teams. Building experience in data analysis, IRB submissions, or clinical trial coordination, and earning a research certification early, positions candidates well for promotion into management within two to four years.
Where can I find and apply to research manager jobs in New Jersey?
You can find and apply to research manager jobs in New Jersey on Migrate Mate, which lists current openings in the state. Find roles that fit your background and apply directly to the ones that interest you.
See All 14 Research Manager Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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