Clinical Research Scientist Jobs in New Jersey
Clinical Research Scientist jobs in New Jersey are among the most active in the country, concentrated in pharmaceutical R&D, oncology, and rare disease research, with openings from entry-level associates through principal scientists and directors. Most hiring is clustered around Princeton, Parsippany, and Newark, where major employers like Johnson & Johnson, Pfizer, and Merck have long-established New Jersey operations. Regulatory science, biostatistics support, and oncology trial management are the specialties commanding the steadiest demand across the state. 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.
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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
See All 7 Clinical Research Scientist Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find JobsClinical Research Scientist Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Clinical Research Scientist Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Science & Research
- Technology & Software
- Biotechnology & Pharmaceuticals
What New Jersey Employers Look For
The qualifications that appear most often in clinical research scientist jobs across New Jersey.
- Bachelor's or advanced degree in life sciences, pharmacology, or a related scientific field
- Experience with clinical trial design, protocol development, and ICH GCP guidelines
- Proficiency in regulatory submission documents including CSRs, IBs, and INDs
- Familiarity with clinical data management systems and EDC platforms such as Medidata Rave
- Strong background in oncology, rare disease, or biologics therapeutic areas preferred
- Ability to collaborate cross-functionally with biostatistics, regulatory affairs, and medical writing teams
Clinical Research Scientist Jobs in New Jersey: Frequently Asked Questions
How do you become a clinical research scientist in New Jersey?
Most clinical research scientists in New Jersey enter the field with a bachelor's degree in biology, chemistry, pharmacology, or a closely related science, though many roles at mid and senior levels expect a master's or doctoral degree. New Jersey does not require a state-issued license specific to this role, but employers strongly favor candidates holding the Association of Clinical Research Professionals certification or the Society of Clinical Research Associates credential, both of which are nationally recognized and widely referenced in New Jersey postings.
Which companies hire clinical research scientists in New Jersey?
Employers hiring clinical research scientists in New Jersey right now include Merck, Red Nucleus, and Syneos Health, based on current listings on Migrate Mate as of August 2026. New Jersey's dense concentration of pharmaceutical and biotech headquarters means that many of these opportunities sit within global drug development organizations rather than smaller contract research organizations.
Which New Jersey cities have the most clinical research scientist jobs?
The cities with the most clinical research scientist openings in New Jersey are Rahway, Princeton, and Parsippany. This distribution reflects New Jersey's pharmaceutical corridor, where major company campuses and R&D centers anchor hiring in the Princeton and Parsippany areas, while Newark draws roles tied to academic medical centers and hospital-sponsored trials at institutions like Rutgers and University Hospital.
Are there remote clinical research scientist jobs in New Jersey?
Yes, and more than many clinical roles, because a meaningful portion of the work involves data review, regulatory writing, and protocol development that can be done off-site. About 50% of clinical research scientist openings tied to New Jersey are remote or hybrid as of August 2026, reflecting the shift many pharmaceutical companies have made since the pandemic. The most remote-compatible tasks are regulatory document preparation, data monitoring review, and cross-functional scientific writing.
How can I get hired as a clinical research scientist in New Jersey with little or no experience?
The most realistic entry path is a clinical research associate or study coordinator role, which several large New Jersey pharmaceutical employers use as a structured pipeline into scientist-level positions. Johnson & Johnson and Merck both run formal early-career development programs in New Jersey that recruit recent science graduates. Completing an internship within a New Jersey-based CRO or academic medical center, combined with earning a clinical research certification, gives candidates a measurable edge over those applying with a degree alone.
Where can I find and apply to clinical research scientist jobs in New Jersey?
You can find and apply to clinical research scientist jobs in New Jersey on Migrate Mate, which lists current openings from employers actively hiring across the state. Search the available roles by location or specialty, find the ones that match your background, and apply directly to the ones that fit.
See All 7 Clinical Research Scientist Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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