Clinical Research Manager Jobs in New Jersey
Clinical Research Manager jobs in New Jersey sit at the center of one of the most active pharmaceutical and life sciences markets in the country, with demand at every level from associate manager through senior director. Most hiring concentrates in the Parsippany, Princeton, and Newark corridors, where companies like Johnson & Johnson, Merck, and Pfizer maintain major operations. The most consistent openings are in oncology trial management, regulatory affairs-adjacent oversight, and multi-site study coordination. 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 45 Clinical Research Manager Jobs in New Jersey
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Find JobsClinical Research Manager Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Clinical 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
- 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 manager jobs across New Jersey.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Minimum five years of clinical research experience with at least two in management
- Certification as a Clinical Research Professional (CCRP) or equivalent credential preferred
- Direct experience managing Phase II through Phase IV clinical trials end to end
- Proficiency with electronic data capture systems such as Medidata Rave or Veeva Vault
- Strong knowledge of ICH-GCP guidelines and FDA regulatory submission requirements
Clinical Research Manager Jobs in New Jersey: Frequently Asked Questions
How do you become a clinical research manager in New Jersey?
Most clinical research managers in New Jersey hold a bachelor's degree in a life sciences, nursing, or health-related field, followed by several years of hands-on trial coordination or monitoring experience. New Jersey does not require a state-issued license for clinical research managers, but employers consistently favor candidates who hold the Society of Clinical Research Associates CCRP certification or the Association of Clinical Research Professionals ACRP-CP credential. Gaining experience at a New Jersey CRO or pharmaceutical company before stepping into management is the most common path.
Which companies hire clinical research managers in New Jersey?
Employers hiring clinical research managers 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 pharmaceutical headquarters and contract research organizations along the Route 1 and I-287 corridors means openings appear consistently throughout the year across both sponsor and CRO sides of the industry.
Which New Jersey cities have the most clinical research manager jobs?
The cities with the most clinical research manager openings in New Jersey are Princeton, Rahway, and Paramus. The distribution follows New Jersey's pharmaceutical belt, where large company campuses and CRO offices cluster around the Princeton and Parsippany areas, while Newark draws openings tied to academic medical centers and hospital-based research programs affiliated with Rutgers and university health systems.
Are there remote clinical research manager jobs in New Jersey?
Yes, and more than many clinical roles, because clinical research managers spend a meaningful share of their time on data review, vendor oversight, and protocol management rather than direct patient contact. About 60% of clinical research manager openings tied to New Jersey are remote or hybrid as of August 2026, reflecting how common flexible arrangements have become across the pharmaceutical and CRO sector. Study monitoring visits and site initiations still require in-person presence, so fully remote roles typically focus on oversight and operations rather than active site management.
How can I get hired as a clinical research manager in New Jersey with little or no experience?
The most realistic entry path is starting as a clinical research coordinator or clinical trial associate at a New Jersey-based CRO or pharmaceutical company, then moving into a team lead or senior coordinator role before pursuing management. Companies like ICON, Syneos Health, and Labcorp Drug Development, all of which have New Jersey operations, regularly hire coordinators and associates without extensive prior experience. Earning the CCRP certification early and building exposure to multiple therapeutic areas, particularly oncology and rare disease given New Jersey's trial volume, strengthens a candidate's case for promotion into a manager title within a few years.
Where can I find and apply to clinical research manager jobs in New Jersey?
You can find and apply to clinical research manager jobs in New Jersey on Migrate Mate, which lists current openings across the state. Search the available roles, find the ones that match your experience and location preferences, and apply directly to each one that fits.
See All 45 Clinical Research Manager Jobs in New Jersey
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