Clinical Research Nurse Jobs in New Jersey
Clinical Research Nurse jobs in New Jersey are in strong demand, concentrated across pharmaceutical and biotech sponsors, academic medical centers, and contract research organizations, with openings at every level from entry-level coordinators supporting trials to senior nurses managing complex oncology and rare-disease protocols. The heaviest hiring is in Princeton, New Brunswick, and Newark, where employers like Johnson & Johnson, Merck, and Hackensack Meridian Health maintain significant research operations. The most sought-after specialties are oncology trials, cardiovascular studies, and early-phase investigational drug research. Find a role that fits below and apply directly.
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The Clinical Research Scientist will be responsible for the development of post-market clinical research strategies of orthopedic devices to support global regulatory and post-market surveillance requirements.
Responsibilities include:
- Work closely with cross-functional teams (Clinical, Medical, Regulatory, R&D, Marketing) to develop post market clinical evidence generation strategies that consider evidence needs for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross functional team to align clinical evidence strategies, document / track decisions and risks, and write PMCF Plans.
- Develop and write high quality Post-market Clinical Follow-up (PMCF) plans and reports with minimal supervision. Support development and drafting of clinical study protocols, registry plans, epidemiology studies, informed consents, investigator brochures, and other study materials where needed.
- Review summaries of clinical evidence and PMCF strategies in other areas of the Technical Documentation for accuracy and completeness. This includes the Clinical Evaluation Plan, Clinical Evaluation Report (CEP), Post Market Surveillance Plan and Periodic Safety Update Report (PSUR).
- Where required, foster relationships with surgeons, hospitals and research teams to gain input into study design, evaluate study feasibility, and identify sites for study execution or data collection. Develop strong collaborative relationships with the study core team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders.
- Partner with the Contracts and Payments team to ensure timely execution of all study agreements and corresponding payments for achieved milestones and deliverables.
- Support clinical scientific discussions with internal stakeholders within Clinical, Medical, Regulatory, R&D and Marketing to drive support of the clinical and regulatory strategy, communicate evidence needs.
- Contribute to appropriate interpretation and dissemination of all evidence generated, including abstracts, manuscripts, and Clinical Study Reports (CSR), epidemiology study results and clinical literature.
- Develop a strong understanding of the orthopedic device product portfolio and business needs for clinical evidence to meet regulatory requirements.
Qualifications:
- A Master’s degree in Biological Science or related discipline, with a minimum of 4 years’ experience in the medical device industry or healthcare field is required
- Advanced technical writing skills is required, with demonstrated experience in writing PMCF plans / reports strongly preferred.
- Clinical expertise in the medical device sector
- Proven experience in conducting clinical studies, registries particularly in the field of orthopaedics
- Strong project management skills required, with demonstrable track record of success managing multiple projects simultaneously with minimal supervision.
- Excellent communication skills, including effective interaction with healthcare professionals (HCPs), hospital staff etc.
Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit. We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status.
To learn more about working at Red Nucleus, please visit Careers | Red Nucleus.
#LI-KS1
The Clinical Research Scientist will be responsible for the development of post-market clinical research strategies of orthopedic devices to support global regulatory and post-market surveillance requirements.
Responsibilities include:
- Work closely with cross-functional teams (Clinical, Medical, Regulatory, R&D, Marketing) to develop post market clinical evidence generation strategies that consider evidence needs for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross functional team to align clinical evidence strategies, document / track decisions and risks, and write PMCF Plans.
- Develop and write high quality Post-market Clinical Follow-up (PMCF) plans and reports with minimal supervision. Support development and drafting of clinical study protocols, registry plans, epidemiology studies, informed consents, investigator brochures, and other study materials where needed.
- Review summaries of clinical evidence and PMCF strategies in other areas of the Technical Documentation for accuracy and completeness. This includes the Clinical Evaluation Plan, Clinical Evaluation Report (CEP), Post Market Surveillance Plan and Periodic Safety Update Report (PSUR).
- Where required, foster relationships with surgeons, hospitals and research teams to gain input into study design, evaluate study feasibility, and identify sites for study execution or data collection. Develop strong collaborative relationships with the study core team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders.
- Partner with the Contracts and Payments team to ensure timely execution of all study agreements and corresponding payments for achieved milestones and deliverables.
- Support clinical scientific discussions with internal stakeholders within Clinical, Medical, Regulatory, R&D and Marketing to drive support of the clinical and regulatory strategy, communicate evidence needs.
- Contribute to appropriate interpretation and dissemination of all evidence generated, including abstracts, manuscripts, and Clinical Study Reports (CSR), epidemiology study results and clinical literature.
- Develop a strong understanding of the orthopedic device product portfolio and business needs for clinical evidence to meet regulatory requirements.
Qualifications:
- A Master’s degree in Biological Science or related discipline, with a minimum of 4 years’ experience in the medical device industry or healthcare field is required
- Advanced technical writing skills is required, with demonstrated experience in writing PMCF plans / reports strongly preferred.
- Clinical expertise in the medical device sector
- Proven experience in conducting clinical studies, registries particularly in the field of orthopaedics
- Strong project management skills required, with demonstrable track record of success managing multiple projects simultaneously with minimal supervision.
- Excellent communication skills, including effective interaction with healthcare professionals (HCPs), hospital staff etc.
Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit. We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status.
To learn more about working at Red Nucleus, please visit Careers | Red Nucleus.
#LI-KS1
See All 44 Clinical Research Nurse Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Clinical Research Nurse JobsClinical Research Nurse Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Clinical Research Nurse Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Chemicals & Materials
- Consulting & Professional Services
- Education
- Medical Devices
- Science & Research
What New Jersey Employers Look For
The qualifications that appear most often in clinical research nurse jobs across New Jersey.
- Active registered nurse license issued or recognized by the New Jersey State Board of Nursing
- Bachelor of Science in Nursing or higher degree from an accredited program
- Experience conducting or coordinating clinical trials under ICH-GCP guidelines
- Certification as a Clinical Research Coordinator or Clinical Research Associate is preferred
- Familiarity with FDA regulations, IND requirements, and IRB submission processes
- Proficiency with electronic data capture systems such as Medidata Rave or Oracle Clinical
Clinical Research Nurse Jobs in New Jersey: Frequently Asked Questions
How do you become a clinical research nurse in New Jersey?
You must hold an active registered nurse license from the New Jersey State Board of Nursing, which requires passing the NCLEX-RN exam after completing an accredited nursing program. Most employers in New Jersey expect a BSN at minimum. From there, candidates typically gain clinical experience in an acute care or specialty setting, then transition into a trial support role, often earning Good Clinical Practice certification to signal readiness for research environments.
Which companies hire clinical research nurses in New Jersey?
Employers hiring clinical research nurses in New Jersey right now include Merck, Colgate-Palmolive, and Cooper University Healthcare, based on current listings on Migrate Mate as of August 2026. New Jersey's dense concentration of global pharmaceutical headquarters and major academic health systems makes it one of the most consistently active states for this role year-round.
Which New Jersey cities have the most clinical research nurse jobs?
Princeton, Rahway, and Paramus have the most clinical research nurse openings in New Jersey. The Princeton and New Brunswick corridor is driven by the headquarters and research campuses of major pharmaceutical companies, while Newark's activity reflects the research programs at RWJBarnabas Health and University Hospital, pulling openings into the broader northeast part of the state.
Are there remote clinical research nurse jobs in New Jersey?
Yes, but they're rare. About 57% of clinical research nurse openings tied to New Jersey are remote or hybrid as of August 2026, reflecting the hands-on nature of most trial work, which requires direct patient contact, specimen handling, and on-site protocol adherence. The portions of the role most likely to be performed remotely are data review, regulatory documentation, and remote site monitoring for sponsor-side positions.
How can I get hired as a clinical research nurse in New Jersey with little or no experience?
The most realistic entry path is a new-graduate or fellowship program at one of New Jersey's large academic health systems, such as those run within RWJBarnabas Health or Atlantic Health System, which place new nurses into research-adjacent roles before full trial assignments. Lateral moves from bedside oncology, infusion nursing, or ambulatory care nursing are commonly accepted because they demonstrate the patient assessment and documentation skills trial sponsors require. Earning a Good Clinical Practice certification before applying gives candidates a clear edge.
Where can I find and apply to clinical research nurse jobs in New Jersey?
You can find and apply to clinical research nurse jobs in New Jersey on Migrate Mate, which lists current New Jersey openings from employers actively hiring. Search the available roles, find the ones that match your experience and specialty, and apply directly to each listing without creating a profile or signing up first.
See All 44 Clinical Research Nurse Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Clinical Research Nurse Jobs