92 Results for

1st Shift Research Jobs in New Jersey

Jobs

New!

Somerville, NJ4 days ago

$18–$20 Per Hour

Perform visual inspection for visible defects of components produced in the Filling Area and components being placed into kits in the Packaging Area. This is an exciting opportunity to join Our Client, a global leader in biotechnology and pharmaceutical research, development and patient care initiatives that help millions of people every day.

Eatontown, NJ14 days ago

You'll keep our production operations running uninterrupted by thoroughly inspecting, diagnosing, repairing, and maintaining equipment to prevent breakdowns and ensure optimal functioning. We continuously analyze our customers' needs within the rapidly evolving payment sector to ensure they always receive secure and innovative services.

Pennsauken, NJ30 days ago

Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. At Cooper University Health Care, our commitment to providing extraordinary health care begins with our team.

Moorestown, NJ30+ days ago

Camden, NJ30+ days ago

Hackensack, New Jersey13 days ago

Responsibilities: Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. Performs nursing assessments and monitors study patient`s progress during clinical trials; Tracks study patient`s response by documenting on toxicity flow sheet, medication flow sheet and nurses` progress notes.

Nutley, New Jersey22 days ago

The Center for Discovery and Innovation- CDI was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases. Qualifications: Education, Knowledge, Skills and Abilities Required: Bachelor's degree in a science or healthcare related field or 2 years equivalent experience and High School diploma, general equivalency diploma (GED), and/or GED equivalent programs.

New!

Paramus, New Jersey2 days ago

Schedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit. Responsibilities: A day in the life of a Clinical Research Coordinator at Hackensack Meridian Health includes: Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.

Hackensack, New Jersey30+ days ago

Neptune, New Jersey30+ days ago

Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. Performs nursing assessments and monitors study patient`s progress during clinical trials; Tracks study patient`s response by documenting on toxicity flow sheet, medication flow sheet and nurses` progress notes.

Princeton, New Jersey17 days ago

We will assess the specific title and level of entry during the interview and assessment process since the actual salary offer will be based on a number of factors, including but not limited to the candidate’s qualifications, experience, skills, and competencies for the role. As a Clinical Research Associate with experience managing clinical trial sites, the number years and type of monitoring experience will determine CRA level.

Princeton, NJ30+ days ago

Full-time

Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites. Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).

Nutley, New Jersey30+ days ago

The Senior Research Associate communicates study progress, data updates, and findings to clinical teams in a clear and actionable manner, and collaborates with clinical departments to integrate behavioral and implementation science research protocols into real-world care settings. The Center for Discovery and Innovation- CDI was established by Hackensack Meridian Health (HMH) as an academic basic and translational research enterprise to rapidly translate science innovation to the clinic and to improve outcomes for patients with cancer, infectious diseases, autoimmune disease and other acute and chronic diseases.

Plainsboro Township, New Jersey29 days ago

$115,000–$130,000 Per Year

Train and support external trial staff regarding CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability, temperature monitoring, query resolution, essential document collection, and ITF filing. Collaborate with Local Trial Manager (LTM) and Line of Business Manager, communicating site progress and escalating critical issues impacting trial milestones.

Princeton, NJ20 days ago

The Research Associate provides independent technical support to research projects with minimal guidance from senior staff, supports the coordination and execution of the scope of work of research projects, participates in coordinating staff efforts across multiple roles (e.g., research assistants, scientists, data analysts, engineers, program administrators, directors, etc.), and contributes as a co-author to presentations or publications. Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide.

Hackensack, New Jersey30+ days ago

The posted rate of pay in this job posting is a reasonable good-faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package. This unique dual-role position combines cutting-edge basic and translational transplant/immunology research with clinical excellence in nephrology, caring for pre- and post-renal transplant patients and living kidney donors.

Princeton, NJ30+ days ago

$64,000–$74,000 Per Year

Through strategic acquisitions, we've expanded our global capabilities: PSI strengthens our workforce assessment solutions, while Edusoft, Kira Talent, Pipplet, Vericant, and Wheebox enhance our educational technology and assessment platforms across critical markets worldwide. Through ETS Research Institute and ETS Solutions, we're partnering with educational institutions, governments, and organizations globally to promote skill proficiency, empower upward mobility, and unlock opportunities for everyone, everywhere.

New!

Princeton, NJ6 days ago

Full-time

Camden, New Jersey7 days ago

The regulatory demands of managing the study portfolio requires a lead position in order to oversee regulatory operations and train new staff members. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.

Hackensack, New Jersey23 days ago

Overview: The Advanced Practice Nurse (APN) utilizes a patient-centered coordinated care model, demonstrating competencies in leadership, direct clinical practice, consultation/collaboration, coaching/guiding, research, and ethical decision-making. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.

Camden, NJ14 days ago

The ideal candidate will have prior experience in a biological research laboratory and experience working with rodents in a wet lab setting • Ability to analyze research results using statistical software• Demonstrated computer skills and proficiency with MS Office suite or similar spreadsheet, database, word processing and presentation software• Ability to work in a collaborative, team-oriented environment, and strong communication skills are required• Ability to work early mornings, evenings, and weekends to administer study protocols, as necessary. • Maintaining, collecting and preparing records of data as well as results for presentations, papers, etc.• Processing the clinical samples such as embedding, section and staining using HE or IHC as needed• Maintaining a mouse colony, contributing experimentally to ongoing research projects and overseeing general laboratory operations and laboratory supplies• Training residents or fellows under supervision in research methods and procedures as needed• Performing other duties as assigned.

Camden, NJ30+ days ago

Working knowledge of general principles in genetics and molecular biology, as well as accurate and timely record keeping, careful organization, and demonstrated interest in working in a laboratory setting is needed to excel in this role• Have prior experience in a biological research laboratory and experience working with rodents in a wet lab setting • Ability to analyze research results using statistical software• Demonstrated computer skills and proficiency with MS Office suite or similar spreadsheet, database, word processing and presentation software• Ability to work in a collaborative, team-oriented environment, and strong communication skills are required• Ability to work early mornings, evenings, and weekends to administer study protocols, as necessary. Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, continuing reviews, amendments, and maintenance of study budget.

Piscataway, NJ17 days ago

$250,000–$275,000 Per Year

Develop new clinical indices and biochemical assessments and apply a broad range of established dental assessment indices (e.g., caries, plaque, gingivitis, periodontology, sensitivity, whitening, calculus, oral malodor, anti-bacterial or others) to design, evaluate, and differentiate clinical programs and product performance that are superior to, existing products. The ideal candidate is an internationally renowned expert in oral health and dental clinical research, with substantial industry and/or academic experience, a proven track record of leading clinical programs, and demonstrated strength in people leadership and collaborative partnerships.

New!

Hackensack, New Jersey6 days ago

Provides professional consultation, advice, and direction to all levels of HMH staff and corporate sponsors regarding contracting issues such that HMH clinical trial contracts will best meet legal sufficiency, risk management and financial requirements for the HMH research objectives. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.

Hoboken, NJ30+ days ago

Part-time

The SERC/AIRC research center at Stevens Institute of Technology is seeking a highly motivated and detail-oriented Student Research Assistant to join our team. Activities will depend on the projects as assigned and may include the following: Survey Design: Develop and design surveys using qualitative and quantitative methodologies.

Parsippany-Troy Hills, NJ30+ days ago

$150,000–$175,000 Per Year

By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes. Identify gaps in pre-clinical and Phase 1 DDP that could impact Phase 2/3 design and execution timelines for company internal projects as well as programs being evaluated as part of due diligence.

New Brunswick, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. Vitalief partners with Sponsors, CROs, and research sites across the clinical trials ecosystem, delivering consulting and workforce solutions that improve efficiency, reduce costs, and accelerate patient-impacting innovation.

New Brunswick, NJ18 days ago

Remote

Part-time

The ideal candidate brings deep expertise in organizational transformation and change management within complex healthcare and research environments, with a proven ability to drive stakeholder alignment, operational adoption, and sustainable process improvement across multi-site systems. Conduct in-depth interviews with clinical research staff and stakeholders across the clinical trial lifecycle to identify operational gaps, bottlenecks, communication challenges, and improvement opportunities across Oncology and Non-Oncology programs.

New Brunswick, NJ30+ days ago

Remote

Part-time

This role will serve as the primary subject matter expert (SME) for a comprehensive current-state operational assessment across Technology, Organization, Process, People, and Finances, with a strong focus on Non-Oncology programs and cross-system communication effectiveness. Conduct in-depth interviews with clinical research staff and stakeholders across the trial lifecycle to identify gaps, bottlenecks, and improvement opportunities for Non-Oncology operations.

New Brunswick, NJ30+ days ago

Full-time

Responsibilities:Under supervision of clinical research leadership staff, the medical staff, and in collaboration with research nurse staff, performs protocol-specific tasks including patient screening, ordering tests, collecting specimens and study documentation of patient reported responses, relative to various Phase 1 Oncology trials. IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP.

Piscataway, NJ16 days ago

$250,000–$275,000 Per Year

Camden, NJ14 days ago

Prefer Experience in cell culture, microscopy (fluorescence and phase), and biochemical and molecular biology techniques Experience with teaching laboratory techniques to students. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.

Orange, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. As the primary subject matter expert (SME), this leader will collaborate closely with the Vitalief delivery team to design and implement enterprise-level operational initiatives, with a strong emphasis on Non-Oncology programs and enhancing cross-system communication and coordination.

Orange, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. As the primary subject matter expert (SME), this leader will collaborate closely with the Vitalief delivery team to design and implement enterprise-level operational initiatives, with a strong emphasis on Non-Oncology programs and enhancing cross-system communication and coordination.

Lawrenceville, New Jersey30+ days ago

£65,977–£82,472

Experimental techniques could include, but are not limited to, the following: Processing human tissue and blood, Cell-based assays, Flow cytometry, ELISAs/MSD assays, RNA extraction and cDNA synthesis, Gene expression array cards. The qualified candidate will process human samples, maintain the laboratory's biobank (including sample storage and retrieval), and perform a range of experimental procedures under the guidance of senior scientists.

New!

New Brunswick, NJ5 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. This position is ideal for oncology nurses currently working in direct patient care roles, whether in a hospital or outpatient setting, who are interested in transitioning into clinical research.

New!

New Brunswick, NJ5 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. This position is ideal for oncology nurses currently working in direct patient care roles, whether in a hospital or outpatient setting, who are interested in transitioning into clinical research.

New Brunswick, NJ30+ days ago

Remote

Full-time

Proven success in building strong executive-level and C-suite relationships while leading a multi-faceted change process; demonstrated broad-based change management expertise and extensive experience positively influencing change in a variety of complex environments with multiple stakeholders and competing priorities. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

New!

Camden, New Jersey6 days ago

Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Short Description: The Clinical Research Nurse will facilitate preparation of IRB protocol submissions and informed consent forms.

Somerset, NJ21 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

Morristown, NJ30+ days ago

Atlantic Health scored four “A” grades by The Leapfrog Group in its Fall 2025 Hospital Safety Grades, performance measures reflecting errors, accidents, injuries and injections, as well as systems hospitals have in place to prevent harm. In addition, Leapfrog recognized us with an \"A\" hospital safety grade - its highest - twelve consecutive times, and the Centers for Medicare and Medicaid Services awarded us again with its highest five-start rating in 2020.

Camden, NJ29 days ago

Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Responsible for completing and maintaining all study documents, in compliance with IRB, Cooper Health System, sponsor and FDA requirements.

Camden, New Jersey30+ days ago

Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Responsible for completing and maintaining all study documents, in compliance with IRB, Cooper Health System, sponsor and FDA requirements.

Rahway, NJ16 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

New Brunswick, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

Teaneck, NJ30+ days ago

$50,003.20–$67,496 Per Year
Full-time

The Coordinator oversees study activities from start-up through close-out, including regulatory submissions, participant screening and enrollment, study visit coordination, data and document management, and ongoing communication with investigators, sponsors, IRBs, and internal clinical teams. Holy Name is New Jersey's only independent Catholic health system, comprising a 361-bed acute care hospital, a renowned cancer center, a state-of-the-art fitness center, a residential hospice, a prestigious nursing school, and an extensive physician network.

New Brunswick, NJ30+ days ago

Full-time

Deliver high-quality, compassionate, hands-on oncology nursing care while coordinating closely with investigators, clinical teams, and ancillary departments (e.g., pathology, radiology, clinical laboratory, surgery, infusion services) in accordance with study protocols, treatment plans, and Good Clinical Practice (GCP) guidelines. IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR.

Freehold, New Jersey16 days ago

Demonstrates appropriate sample management activities to ensure the integrity of all biological samples; Manages or oversees the inventory of equipment and supplies related to the study and orders more as needed. Under the direction of the Oncology service line director and/or research nurse manager, oversees and directs the clinical course of research participants during clinical trial participation.

Hamilton, NJ30+ days ago

Full-time

Additional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg.

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1st Shift Research Jobs in New Jersey

1st Shift Packaging Associate Tailored Management

1st Shift Maintenance Technician TAG Systems Group

Supply Technician (1st Shift) Cooper University Hospital

Supply Technician (1ST SHIFT) Cooper University Hospital

Supply Tech (1st Shift) Cooper University Hospital

Supply Technician (PER DIEM 1st Shift) Cooper University Hospital

Clinical Research Nurse - Phase 1 - P/T with Benefits - Days Hackensack Meridian Health

Research Associate - Center for Discovery and Innovation- CDI Hackensack Meridian Health

Clinical Research Coordinator Hackensack Meridian Health

Clinical Research Nurse - Children's Hospital - F/T Days Hackensack Meridian Health

Clinical Research Nurse Hackensack Meridian Health

Clinical Research Associate (CRA) – All levels (I/II/Senior) Theradex Oncology

Senior Clinical Research Associate Systimmune

Senior Research Associate, Center for Discovery and Innovation - CDI Hackensack Meridian Health

Senior Clinical Research Associate System One

Research Associate ETS

Transplant Nephrologist, Research Hackensack Meridian Health

Senior Research Assistant ETS

Clinical Research Associate II Systimmune

Research Regulatory Coordinator III Cooper University Hospital

Oncology Myeloma Research Nurse Practitioner John Theurer Cancer Center Hackensack Meridian Health

Research Assistant PRN Cooper University Hospital

Research Assistant-Part Time Cooper University Hospital

Sr. Director, Clinical Research (Piscataway, NJ, US) Colgate-Palmolive Company

Senior Research Contract Specialist - Per Diem Hackensack Meridian Health

SERC/AIRC Student Research Assistant Stevens Institute of Technology

Associate Director Clinical Research & Development Judge Group

Oncology Clinical Research Nurse Director Vitalief

Clinical Research Change Management Consultant Vitalief

Clinical Research Strategic Management Consultant Vitalief

Senior Clinical Research Coordinator Vitalief

Sr. Director, Clinical Research Colgate-Palmolive

Research Associate Cooper University Hospital

Senior Director, Clinical Research Operations Vitalief

Director, Clinical Research Operations Transformation Vitalief

Associate Research Scientist RD Partners

Oncology RN – Clinical Research Nurse (Training Provided) Vitalief

Oncology Nurse (RN) – Clinical Research Career Opportunity Vitalief

Vice President, Clinical Research FSP Consulting Vitalief

Clinical Research Nurse I Cooper University Hospital

Clinical Research Coordinator (CRC) – Infectious Disease Vitalief

Lead Clinical Research Nurse, Part Time Days, 8a - 4p, Atlantic Health, Morristown Medical Center Atlantic Health System

Clinical Research Nurse I - CNI Cooper University Hospital

Clinical Research Nurse II Cooper University Hospital

Clinical Research Coordinator – Cardiovascular Vitalief

Clinical Research Coordinator Vitalief

Clinical Research Coordinator-Full-time-Onsite Holy Name Medical Center

Clinical Research Nurse Vitalief

Research Nurse CentraState Healthcare System

International Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute, LLC

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