612 Results for

Research Jobs in Metuchen, NJ

Jobs

New!

New York, NY4 days ago

$120,000–$140,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations.

Basking Ridge, NJ11 days ago

$100,960–$151,440 Per Year
Full-time

Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Job Description. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.

Jersey City, NJ13 days ago

Collaboration: Develop and nurture professional relationships with physicians and staff at JSUMC and other Hackensack Meridian Health (HMH) campuses, including Ocean University Medical Center (OUMC), to promote practice growth to Bayshore Medical Center (BMC). ? 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.

Summit, NJ17 days ago

$30–$35 Per Year
Full-time
Employee

Work closely with cross-functional teams, including other R&D functions, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals. Prepare and maintain detailed documentation for product development processes, including experimental protocols, and technical reports in compliance with Good Documentation Practices (GDP).

New York, NY15 days ago

$25–$30 Per Hour

The Rogosin Institute is an independent not-for-profit medical care and research organization affiliated with New York Presbyterian Hospital and Weill Cornell Medicine. Under the supervision of a registered nurse, the Clinical Assistant participates in the delivery of patient care services by direct patient care and supportive services.

Newark, NEW JERSEY30+ days ago

Candidates located in Newark, NJ will perform the same essential work as other panel members, with local targeting used to broaden geographic reach while keeping the position itself consistent. As a Virtual Market Research Associate, you will help research teams gather authentic reactions from consumers in Newark and across the United States.

New York City, NY30+ days ago

$34–$44 Per Hour

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).

New York City, NY30+ days ago

$34–$44 Per Hour

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. As a Clinical Research Assistant, PRN (Registered Nurse) you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.

Nutley, New Jersey24 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 Jersey4 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.

New York, NY8 days ago

$53,294.22–$57,750
Temporary

Works with departments, labs, other personnel and areas as needed, to ensure the timely transfer of items and biological materials: study drugs; histology slides; serum, urine, blood samples, etc., using appropriate precautions at all times. Works with School of Medicine and Medical Center staff and departments, including Directors, Managers, Clinical Information Systems, Research Nursing and Regulatory Services; may also interfaces with patients and their families.

New York, NY7 days ago

$53,294.22–$57,750 Per Year

New York City, NY30+ days ago

$20–$25 Per Hour

This role focuses on the hands-on execution of essential administrative and clinical tasks—such as scheduling, preparing visit materials, supporting participant flow, maintaining source documentation, and completing timely data entry—to ensure efficient site operations and high-quality study conduct. The enrollment RA works closely with the enrollment coordinators to provide insights that inform clinical judgment on participant eligibility and study suitability and assists with screening activities and accurate documentation in compliance with ICH-GCP, study protocols, and regulatory requirements.

Hackensack, New Jersey15 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.

Princeton, New Jersey19 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.

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, 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.

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 York City, NY30+ days ago

$85,000–$90,000 Per Year

Oversee investigational product (IP) accountability across all assigned trials, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal; ensure compliance with protocol, regulatory requirements, and site SOPs, and provide guidance and oversight to CRCs and RAs supporting IP management. Serve as the primary operational lead for study start-up activities, including SIV and PSV readiness, document preparation, development of site workflows, staff training completion, and management of study supplies.

Brooklyn, NY30+ days ago

$17–$17

Engage in experiential learning activities at our Brooklyn Clinical Research Center, such as consenting practice, protocol reviews, patient case reviews, and observation of clinical assessments including vitals, phlebotomy, and lab processing to apply theoretical knowledge to real-world research studies. The network also includes 12 community medicine sites providing care to disenfranchised New Yorkers, comprehensive HIV services, chemical dependency programs, and a family support center that offers educational, vocational, and other social support programs.

New York, NY30+ days ago

$70,481.60–$75,428.87 Per Year

Director Clinical Research Finance to prepare Cancer Center expense budgets associated with clinical trials revenue and expense for upcoming fiscal year, based on professional judgment and a projection of direct and indirect costs and fee revenue for open and pending trials. Director Clinical Research Finance, ensures fiscal compliance to trial sponsor and institutional policies and procedures, and ensures that the departments fiscal interests are served in the conducting of oncology clinical trials.

New York City, NY30+ days ago

$31.97–$33.17 Per Year

Maintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs. This role is ideal for coordinators with experience managing one or more trials, supporting day-to-day study operations, and working collaboratively with research staff under guidance from senior team members.

Plainsboro Township, New Jersey30+ 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.

Brooklyn, NY30+ days ago

New York, New York30+ days ago

Overview: Reporting to the Clinical Research Coordinator (NP), the Study Research Coordinator focuses on trial operations and participants, coordinating day-to-day activities and assisting investigators with preparing IRB applications and submitting them to the Diagnostic and Treatment Center (D&TC). The salary of the finalist selected for this role will be set based on various factors, including but not limited to organizational budgets, qualifications, experience, education, licenses, specialty, and training.

Long Island, NY25 days ago

Founded in 2021, SiteBridge Research is an integrated research organization, focused on building a national network of small and community medical practices to deliver world-class industry-sponsored clinical research studies on time and on budget, accelerating time to completing clinical trials, accelerating time to market and product adoption in communities that are often underrepresented and difficult to reach. The SiteBridge Network extends reach further into these communities to empower patients with some of the highest unmet needs to take part in clinical studies to improve inclusivity in clinical research and to improve overall health outcomes.

New!

New York, NY5 days ago

$140,000–$185,000

Actual openings may vary based on employer type (hedge funds, private equity, venture capital, mutual funds, or asset managers) and focus areas (equities, fixed income, private markets, or alternative investments). These roles often involve close collaboration with portfolio managers, investment analysts, risk teams, and senior leadership to provide rigorous research, performance tracking, and market intelligence.

New York, NY30+ days ago

$25.84–$34.06

After a period of time working with the research team, the candidate will be expected to train newly hired Research Associates, graduate students, and postdoctoral fellows in the study design, data collection, blood processing. This is a per diem position with variable hours based on study needs, operational priorities, and candidates availability, offering scheduling flexibility; the role requires availability for early morning shifts (as early as.

New York, New York30+ days ago

$130,000–$150,000 Per Year

This includes developing, leading, and executing new programs and initiatives to grow NYU’s capacity in this area, as well as celebrating successes through events like the Tech Venture Summit to raise the visibility of and engagement in entrepreneurship within NYU’s research community. This role involves actively coaching deep tech teams and serving as a principal liaison to the NY I-Corps Hub, external partners in the deep-tech ecosystem, and key university stakeholders, such as research deans and department chairs.

New!

Parsippany, NJ1 day ago

$178,000–$210,000 Per Year

Responsibilities: Contribute to and support the company’s efforts in communicating the high value of Ferring Uro-oncology research initiatives to successfully execute trial needs Initiate and maintain relationships with study investigators to create advocates for Ferring Uro-Oncology research Collaborate with the Therapeutic area medical team and medical affairs to support current PI involvement and KOL engagement initiatives Uncover opportunities for engagement to ensure appropriate enrollment at each research center Collaborate with Ferring clinical operations, TA medical directors, and CRO to identify and develop key performance indicators (KPIs) for activities aimed at enhancing trial recruitment, and ensure reports are developed and shared with management to track progress and drive improvements Work with Ferring clinical operations, TA Medical Directors and CRO to understand KPIs for enrollment and support where necessary for optimal study performance – then delete this as incorporated in above Work to facilitate collaboration between different departments or groups within the same study site to optimize the enrollment of trial participants, feeding back any trial-specific impact to the Ferring clinical operations team to ensure coordinated efforts Report identified site or vendor issues to Clinical trial team via TA medical directors including opinions and observations related to the operational, scientific and other aspects of the study so that Ferring clinical operations team can assess appropriate trial-related actions Collaborate with Ferring medical affairs and CTT during the start-up phase for selection of sites to enable and retain beneficial experiences and best practices Ensure alignment of medical communications and publications plans within the overall medical brand and development plan – delete as this has too much overlap with existing teams and processes Support and partner with key internal business partner Ensure effective interaction & communication between the uro-oncology research team, medical science liaison teams and other key stakeholders Requirements: Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 15+ years in matrix leadership organizations in operational or client facing environments. Experience working with Urologist preferred Prior medical affairs, medical communications, publications and/or KOL management experience highly desired Proven leadership track record with exceptional communication, collaboration and prioritizing skills, supporting pre and post-launch activities.

New York, NY30+ days ago

$29.55–$29.56
Temporary

The overarching role for the per diem RDA is to provide assistance in the recruitment of research participants, clinical research study visits and procedures, data entry and analyses, and other support duties in compliance with Good Clinical Practice, HIPAA, and required obligations to participants, the PI, research team, and the sponsor. Provides support for federally funded human subjects research investigating treatments for schizophrenia, including recruitment of research participants, management of study folders and databases, and conduct of study assessments (when applicable).

Princeton, NJ22 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.

Brooklyn, NY17 days ago

$25–$35

Demonstrated experience applying core research methods (user interviews, workflow observation, surveys, qualitative and quantitative analysis) in a substantive project, such as a graduate thesis, lab study, applied internship, or industry engagement. Master's or PhD candidate (or recent graduate) in a research-heavy field, for example public health, health informatics, anthropology, behavioral or cognitive science, psychology, human factors, or related.

New York, NY12 days ago

$53,797.97–$53,797.97

Reviews data with supervisor and then provides reports to all parties (e.g., data and safety monitoring committee, the principal investigator, sponsoring agency, etc.) on the progress of the study. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people.

New York, NY30+ days ago

$29.55–$29.56
Temporary

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 York, NY30+ days ago

$25.84–$34.06 Per Hour

Hackensack, New Jersey8 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.

New Brunswick, NJ20 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 York, NY30+ days ago

$100,000–$120,000

The primary purpose of the subspecialized oncology clinical research nurse role is to facilitate positive outcomes of safety and quality for patients enrolled on adult oncology clinical trials at the NYU Perlmutter Cancer Center by coordinating and managing patients enrolled on clinical trials by employing the nursing process, clinical skills, critical thinking, evidence-based nursing and an understanding the scientific research. 2. Utilizing the nursing process, nursing assessment skills and critical thinking the Oncology CRN I conducts a thorough research screening visit for potential trial participants per the protocol requirements, including but not limited to a Review of Systems (ROS), baseline and ongoing AE assessment and documentation, and collection of concomitant medications and documents the assessments in the EPIC electronic health record per CTO policies and procedures.

New!

New York, NY4 days ago

$29.55–$29.56 Per Hour

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.

Hackensack, New Jersey25 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.

New York, NY22 days ago

$43,700–$52,101 Per Year

The Research Assistant will assist with research study procedures, including scheduling of subjects for study procedures, conducting data entry, assisting Principal investigators in study administration, and assisting with contacting research study subjects by phone when needed. A critical component of these efforts is ensuring that RFMH is a diverse and inclusive workplace where all employees' unique attributes and skills are valued and utilized to support the mission of the Agency.

New Brunswick, NJ7 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, NJ7 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.

Princeton, NJ8 days ago

Full-time

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Research Jobs in Metuchen, NJ

Sr. Oncology Clinical Research Associate Jobot

Sr Clinical Study Assoc CO Daiichi Sankyo, Inc.

Urogynecologist Hackensack Meridian Health

Research & Development, Scientist 2 YANTRAN LLC

Clinical Assistant The Rogosin Institute

Virtual Market Research Associate AFG

Clinical Research Assistant, PRN Care Access

Clinical Research Assistant, PRN (Bilingual, Registered Nurse) Care Access

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

Clinical Research Coordinator Hackensack Meridian Health

Clinical Research Assistant NYU Langone Health

Clinical Research Assistant NYU Langone Medical Center

Clinical Research Enrollment Assistant Adams Clinical

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

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

Clinical Research Nurse Hackensack Meridian Health

Senior Clinical Research Associate Systimmune

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

Transplant Nephrologist, Research Hackensack Meridian Health

Senior Research Assistant ETS

Clinical Research Coordinator III Adams Clinical

Intern - Research NYU Langone Health

Financial Coordinator - Clinical Research NYU Langone Medical Center

Clinical Research Coordinator II Adams Clinical

Senior Clinical Research Associate System One

Intern - Research NYU Langone Medical Center

Study Research Coordinator| Diagnostic & Treatment Center Rockefeller University

Clinical Research Coordinator SiteBridge Research, Inc.

Fund Research Associate Career Launch AI

Per Diem Research Associate - Bilingual Spanish Preferred NYU Langone Health

Assistant Director of Research Commercialization New York University

Director, Clinical Research Alliances Ferring Pharmaceuticals, Inc.

Per Diem Research Data Associate NYU Langone Health

Research Associate ETS

Clinical Product Research Intern Norbert Health

Research Data Associate NYU Langone Health

Research Data Associate, Temporary Per Diem Full Time NYU Langone Health

Oncology Clinical Research Nurse Director Vitalief

Per Diem Research Associate - Bilingual Spanish Preferred NYU Langone Medical Center

Senior Research Contract Specialist - Per Diem Hackensack Meridian Health

Clinical Research Change Management Consultant Vitalief

Clinical Research Strategic Management Consultant Vitalief

Clinical Research Nurse I - Oncology NYU Langone Health

Per Diem Research Data Associate NYU Langone Medical Center

Senior Clinical Research Coordinator Vitalief

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

Research Assistant New York State Psychiatry Institute

Oncology RN – Clinical Research Nurse (Training Provided) Vitalief

Oncology Nurse (RN) – Clinical Research Career Opportunity Vitalief

Clinical Research Associate II Systimmune

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