1,129 Results for

Clinical Jobs in New Jersey

Jobs

Parsippany-Troy Hills, NJ

Full time

The right candidate will possess strong organizational and problem-solving skills with attention to detail and excellent communication skills, who can translate between technical and non-technical stakeholders. This role sits at the intersection of information systems, software development, and operations, driving delivery of web-based clinical platforms used for medical imaging review and data workflows.

4 days ago

Basking Ridge, NJ

$127,280–$190,920 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF.

Become a Subject Matter Expert (SME) with the process currently in use; be able to describe to study teams and other key departments how their study will interact with the adjudication vendor;

Describe the expectation and importance of adjudication between the vendor to the CRO;

Become an active “extended team member” to multiple studies at the same time; Being extremely organized to discuss with studies at different timepoints.

24 days ago

Basking Ridge, NJ

$100,960–$151,440 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. 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.

30+ days ago

Princeton, NJ

$85,000–$143,000 / year

Facilitate timely workup of patients for access management, dialysis services, patient education, hospitalizations, and kidney transplantation as appropriate, and ensures coordination of care with the multidisciplinary renal team.

Frequently interacts with subordinate supervisors, customers, and/or functional peer group managers, normally involving matters between functional areas, other company divisions or units, or customers.

4 days ago

Basking Ridge, NJ

$136,080–$204,120 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF.

CRO Oversight: Responsible for the oversight, performance, and management of CRO(s) and 3rd party vendors (sub-contracted by CRO) to ensure compliance with Daiichi Sankyo’s quality measures and adherence to scope of work within timelines and budget at a task level.

30+ days ago

Basking Ridge, NJ

$136,080–$204,120 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF.

4 days ago

Cherry Hill Mall, NJ

Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University , home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.

1 day ago

Basking Ridge, NJ

$162,400–$243,600 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. This position requires minimal supervision to provide critical study-level support to the CSL/PS/MM/GCL for the successful execution of assigned studies.

Responsibilities.

4 days ago

Berkeley Heights, NJ

$50,000–$55,000 / year

Lantern Hill helps people live better lives by fulfilling our promises of a vibrant lifestyle, financial stability, and focused health and well-being services for those who live and work with us. See Erickson Senior Living Privacy Policy at https://www.ericksonseniorliving.com/privacy-policy and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions.

3 days ago

New Brunswick, NJ

$100,000–$125,000

Learn more about working here at http://www.aramarkcareers.com or connect with us on Facebook, Instagram and Twitter. For more information about Aramark benefits, click here Aramark Careers - Benefits & Compensation.

8 days ago

Basking Ridge, NJ

$153,600–$230,400 / year
Full time

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Leadership, Direction, and Strategy:

Establish programming strategy in designing, developing, and maintaining reporting business needs, including programming capabilities assessment, technology and infrastructure requirements of new and/or existing clinical database applications and reporting solutions.
Project Management:
- Drive successful delivery of clinical data management programming objectives by aligning priorities, streamlining workflows, and optimizing resources in collaboration with cross-functional stakeholders.

30+ days ago

Basking Ridge, NJ

$242,700–$404,500 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF. Lead scientist team to collaborate with safety physicians, regulatory affairs, clinical development, other functions and external partners to deliver high-quality safety assessments, regulatory submissions, aggregate reports, and responses to health authority queries.

30+ days ago

Somerset, NJ

$100,000–$120,000 / year

Our client is a growing multi-site healthcare practice operating across New Jersey and New York, providing comprehensive clinical services and working closely with physicians, legal offices, vendors, and specialized care providers. The highly organized and proactive Clinical Operations Managerwill serve as the central hub supporting physicians, clinical staff, office operations, and external partners.

Today

Oceanport, NJ

$121,935–$156,140 / year

p>Monmouth Medical Center (MMC) stands as one of New Jersey's largest community teaching hospitals, where a collaborative team of physicians and staff is dedicated to achieving excellence in both academic and clinical settings, while providing compassionate patient care.

For over 130 years, MMC has been a leader in central New Jersey, delivering top-notch healthcare and the latest medical technologies to nearly one million residents in Monmouth County and parts of Ocean and Middlesex counties.

1 day ago

Basking Ridge, NJ

$201,840–$302,760 / year
Full time

p style="margin:0in;line-height:normal;font-size:12pt;font-family:'aptos' , sans-serif">Download Our Benefits Summary PDF.

Oversee RBQM activities for Daiichi Sankyo Portfolio of Studies: Serve as senior level technical RBQM SME and oversee Central Risk Managers to ensure proper implementation and execution of RBQM and inspection readiness.

10 days ago

Secaucus, NJ

li>Performs study procedures (e.g., obtain ECG recordings, vital signs, safety assessments, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

30+ days ago

Bridgewater, New Jersey

Remote

p>To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Clinical Data Managers for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.

Is responsible for planning and implementing data management timelines and deliverables; and is responsible for providing database and data management activities status reports; contributes to the overall project planning, progress tracking and reporting.

30+ days ago

Parsippany, Kansas

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

30+ days ago

Parsippany, New Mexico

p>As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing study‑related procedures, and ensuring adherence to study protocols and regulatory requirements. This role is well‑suited for a detail‑oriented research professional who enjoys direct patient interaction, values data integrity, and is committed to high‑quality clinical research within diverse communities.

3 days ago

Neptune, New Jersey

li>Ensures timely, accurate, and reliable documentation, tracking, and reporting of all required clinical trial study and patient data and metrics through routine collaboration with all research team members including but not limited to Investigators, Clinical Research Nurses, Clinical Research Coordinators, Regulatory and Study Start-Up Specialists, Clinical Data Coordinators, Study Contract and Finance Staff, Sponsors and Contract Research Organizations, and other team members throughout the HMH Network as required.

Focuses on continuous process improvement strategies both within the assigned Research Program or Division and throughout the entire HMH Research Enterprise, always seeking opportunities for streamlining and/or accelerating accruals to clinical trials, data cleaning, data quality, and trial completion.

18 days ago

Morristown, NJ

$178,500–$257,833.33 / year

p>The position combines strong digital and AI domains with function-level business and transformation leadership, requiring the ability to produce decision-grade insights for CSO leadership, translate complex technology and regulatory constraints into strategic value hypotheses, and steer outcomes across highly matrixed, regulated environments.

Direct and validate: Competitive and technology intelligence to inform strategic positioning, function-level business needs and value hypotheses, prioritization of business-driven requirements shaping product and roadmap decisions & gaps analysis against existing solutions and operating models.

30+ days ago

Parsippany, Kansas

The CRC will play a critical role in study coordination, patient engagement, clinical procedures, and data management while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

17 days ago

Toms River, NJ

By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.

30+ days ago

Clifton, NJ

Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

30+ days ago

Secaucus, NJ

$20–$22 / hour

Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Title: Clinical Research Administrative Assistant Location: Secaucus, NJ Reports To: Senior Vice President.

30+ days ago

New Jersey

Remote

p>Everest Clinical Research (“Everest”) is a full-service, global, contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.

Follow up on regulatory requirements, industry trends, benchmarking, and best working practices in data management and database design by reading, participating in relevant training, and/or associated activities.

30+ days ago

Parsippany, California

The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

30+ days ago

Parsippany, South Dakota

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

10 days ago

New Jersey

Remote

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Develop new features and functionality within the database design functional areas to increase the efficiency of database design at the study level, and to improve and enhance the company’s database design capabilities.

30+ days ago

Mahwah, NJ

Leading people who perform project management duties involving cross-functional teams focused on delivering internal products or administrative systems. Organizing project activities and interdepartmental meetings, ensuring communication facilitates the completion of the program or project on schedule and within budget constraints.

24 days ago

p>A day in the life of a Clinical Research Nurse at Hackensack Meridian Health includes:

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.
The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

30+ days ago

Parsippany, Pennsylvania

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

30+ days ago

New Brunswick, NJ

MISSION: Our mission is to accelerate scientific discovery focused on understanding cancer, innovating cancer treatment, and improving cancer prevention; to provide outstanding, novel, and compassionate patient care; to provide evidence-based and culturally informed education to physicians, nurses, researchers, staff, and the community; and to achieve cancer health equity in our state through outreach to and engagement of our extraordinarily diverse communities. The purpose of the Manager Contract Management (Clinical Research) position is to foster mutually beneficial strategic alliances between Rutgers University and clinical research industry sponsors, to benefit of the sponsors, New Jersey, and the general public through professional and responsive review, negotiation, and management of clinical trials and associated clinical research agreements, on behalf of Rutgers Cancer Institute and its faculty.

30+ days ago

Hackensack, NJ

Hackensack Meridian Health nurses care for patients and their families at every stage of life, 24 hours a day, at bedsides in 9 community hospitals, 4 academic medical centers, a behavioral health hospital, 2 children's hospitals, 2 rehabilitation hospitals, medical offices, and care facilities across the state. 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.

30+ days ago

$142,400–$224,100 / year

or B.S. degree, preferably in life sciences, computer science, or related discipline, with at least 6 years' experience in Clinical Data Management or a mix between Data Management and Clinical Research and at least 3 years' experience working with formal project management tools and processes.

The Principal Trial Manager is responsible for leading projects and initiatives to improve the quality and compliance of the data management functional areas in addition to the regular responsibilities as an individual Trial Manager (TM).

8 days ago

Hackensack, New Jersey

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.
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.

11 days ago

Morristown, NJ

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. The SPA I oversees the quality review and accuracy of Clinical Trial Agreements and Budgets and is responsible for tracking reports and perspective for refinement of operational activity in the Atlantic Health Clinical Research & Innovation Institute.

13 days ago

Newark, NJ

Aligned with Rutgers UniversityNew Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and five centers and institutes that focus on cancer treatment and research, neuroscience, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research. Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption.

30+ days ago

Piscataway, NJ

$250,000–$275,000 / year

p>Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under such internationally recognized brand names as Colgate, Palmolive, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom's of Maine, Sanex, Ajax, Axion, Soupline, Haci Sakir, Suavitel, PCA SKIN, EltaMD, Filorga and Hello as well as Hill's Science Diet and Hill's Prescription Diet.

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.

24 days ago

Hackensack, New Jersey

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.
The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

30+ days ago

$310,900–$489,400 / year

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Working closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility.

Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.

30+ days ago

Parsippany, Georgia

In this remote role you will serve as the primary country-level leader for clinical trial delivery, ensuring studies are executed efficiently from start-up through closeout. Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target.

18 days ago

Rahway, NJ

$117,000–$184,200 / year

p>Co-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts.

Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.

2 days ago

Hackensack, New Jersey

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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.

The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

14 days ago

Neptune, New Jersey

p style="margin:0in"/> 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.
The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials.

3 days ago

New Brunswick, NJ

Remote

Part time

30+ days ago

East Brunswick, New Jersey

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Clinical Jobs in New Jersey

Job Description.

Responsibilities.

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Clinical Jobs in New Jersey

Technical Project Manager – Clinical Systems Canfield Scientific, Inc.

Manager, Clinical Adjudication Operations Daiichi Sankyo, Inc.

Sr Clinical Study Assoc CO Daiichi Sankyo, Inc.

Job Description.

Dialysis Clinical Manager Registered Nurse - RN Fresenius Medical Care

Clinical Study Manager, Clinical Operations Daiichi Sankyo, Inc.

Clinical Study Manager, Global Clinical Operations Daiichi Sankyo, Inc.

CT Technician - CVT - Clinical Supervisor - Cath / EPS Lab - Full Time - Jefferson Einstein Philadelphia Jefferson Health

Associate Director, Clinical Science Daiichi Sankyo, Inc.

Responsibilities.

Registered Clinical Dietitian Lantern Hill by Erickson Senior Living

Clinical Nutrition Manager Aramark

Associate Director, Clinical Database Applications and Reporting Daiichi Sankyo, Inc.

Senior Director, Clinical Safety Scientist Daiichi Sankyo, Inc.

Clinical Operations Manager Atrium

Assistant Director Clinical-Mother Baby Full Time NIght Monmouth Medical Center

Director, Risk Based Quality Management (RBQM) Daiichi Sankyo, Inc.

Assistant Clinical Research Coordinator/Equipment Supervisor Frontage Clinical Services Inc

Senior Clinical Data Manager Everest Clinical Research

Clinical Research Associate - Sponsor Dedicated IQVIA

Clinical Research Coordinator - Albuquerque, NM IQVIA

Project Manager, Clinical Trials Hackensack Meridian Health

Clinical Digital & AI Acceleration Innovation Manager Sanofi

Clinical Research Coordinator - Wichita, KS IQVIA

Clinical Research Coordinator II - Toms River, NJ Iterative Scopes Inc

Clinical Research Coordinator II Iterative Scopes Inc

Clinical Research Administrative Assistant Frontage Clinical Services Inc

Clinical Database Designer I Everest Clinical Research

Clinical Research Coordinator - Loma Linda, CA IQVIA

Clinical Research Coordinator - Sioux Falls, SD IQVIA

Senior Clinical Database Designer I Everest Clinical Research

Clinical Research Project Manager iMPact Business Group

Clinical Research Nurse Hackensack University Medical Center

Clinical Research Coordinator - Philadelphia, PA IQVIA

Manager Contract Management (Clinical Research) Rutgers The State University of New Jersey

Clinical Research Nurse - Phase 1 - F/T - Days Hackensack University Medical Center

Assoc. Dir, Clinical Data Mgmt (Hybrid) Merck & Co Inc

Clinical Research Coordinator Hackensack Meridian Health

Sponsored Projects Analyst I - Atlantic Health Clinical Research & Innovation Institute Atlantic Health System Inc

Clinical Research Coordinator II Rutgers The State University of New Jersey

Sr. Director, Clinical Research Colgate-Palmolive Co

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

Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma Merck & Co Inc

Clinical Project Lead, Oncology IQVIA

Senior Scientist, Clinical Research Merck & Co Inc

Clinical Research Nurse Hackensack Meridian Health

Clinical Research Nurse - JS Hope Tower - F/T Days Hackensack Meridian Health

Clinical Research Change Management Consultant Vitalief

Clinical Research Coordinator Astera Cancer Care

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

Clinical Research Coordinator Sr. CenExel

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