Registered Nurse Clinical Specialist, Full Time, Operating Room, Atlantic Health Morristown Medical Center Atlantic Health SystemRegistered Nurse Clinical Specialist, Full Time, Operating Room, Atlantic Health Morristown Medical CenterMorristown, NJAtlantic 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.
Clinical Account Representative, CardioMEMS - Eastern Region AbbottClinical Account Representative, CardioMEMS - Eastern RegionNewark, New Jersey$68,000–$136,000 / yearWe’re looking for high-performing, clinically experienced sales professionals with deep cardiovascular expertise to drive adoption and growth of CardioMEMS across multiple locations (Lexington, KY, Louisville, KY, Augusta, GA, New Jersey, Philadelphia, PA and Dayton, OH) through strategic account development, education, and partnership. The CAR operates at the intersection of clinical expertise, relationship management, and commercial execution, ensuring that CardioMEMS is successfully integrated into heart failure care pathways and delivers measurable patient and economic value.
Associate Director, Global Medical Cardiovascular, Mavacamten Bristol-Myers Squibb CoAssociate Director, Global Medical Cardiovascular, MavacamtenPrinceton, NJ$166,350–$201,571 / yearThis role provides scientific and clinical leadership across global deliverables-including core content and scientific materials, congress planning support, medical education, and cross-functional scientific engagement-to ensure timely, high-quality support for US priorities and milestones. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
NewGlobal Medical Affairs Leader (GMAL), Lung Johnson & JohnsonGlobal Medical Affairs Leader (GMAL), LungRaritan, New JerseyAnalytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Customer Analytics, Design Mindset, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Strategic Thinking, Tactical Thinking, Technical Credibility . As the leader of the WWMAST (Worldwide Medical Affairs Strategy team), the GMAL will work with the Regional Medical Affairs Leaders in addressing data gaps and building confidence to ensure the most optimal and safe use of amivantamab and lazertinib and maximize the benefit for patients.
Clinical Nurse Specialist -Med/Surg - Per Diem Days Hackensack University Medical CenterClinical Nurse Specialist -Med/Surg - Per Diem DaysNJAs a knowledgeable practitioner, the Clinical Nurse Specialist demonstrates positive behavior and the ability to perform ongoing clinical assessment of the patient, establishes and implements a plan of care, and evaluates the outcome of that care, utilizing the nursing process. As a researcher, the Clinical Nurse Specialist utilizes the research process to promote quality patient care, promote the growth of knowledge in the nursing profession, and support evidence-based practice, and safety and quality improvement.
Clinical Services Manager (Mcs) DaVita Inc.Clinical Services Manager (Mcs)West Orange, NJ$95,000–$135,000 / yearProfessional development programs: DaVita offers a variety of programs to help strong performers grow within their career and also offers on-demand virtual leadership and development courses through DaVita's online training platform StarLearning. Participates with the Regional Director and Facility Administrator in the proactive identification and development of facility specific education and outcome goals including: implementation and monitoring of the goals to achieve desired results.
Senior Director, Global Medical Oncology, Pumitamig Breast Cancer and Other Rare Tumors Bristol Myers SquibbSenior Director, Global Medical Oncology, Pumitamig Breast Cancer and Other Rare TumorsPrinceton, NJ$229,380–$277,956 / yearThe role supports the development and implementation of the Global/US Pumitamig Medical Plan, leads or collaborates within Alliance Medical and cross-functional forums which includes the development of Integrated Evidence Plans (IEPs), scientific narratives, publication plans, congress strategies, field medical trainings, and external engagements. In collaboration with Global Medical Evidence Generation Team and within the Alliance partnership, develops and executes the integrated evidence generation plan (IEP), including Medical Affairs Pumitamig breast cancer and other rare tumors trials, and evaluation of Pumitamig breast cancer and other rare tumors investigator-initiated or collaborative trials.
Senior Director, Global Medical Oncology, Pumitamig GI/GU Cancers Bristol Myers SquibbSenior Director, Global Medical Oncology, Pumitamig GI/GU CancersPrinceton, NJ$229,380–$277,956 / yearThe role supports the development and implementation of the Global/US Pumitamig Medical Plan, leads or collaborates within Alliance Medical and cross-functional forums which includes the development of Integrated Evidence Plans (IEPs), scientific narratives, publication plans, congress strategies, field medical trainings, and external engagements. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
NewSenior Global Medical Affairs Leader - H&N Cancer Johnson & JohnsonSenior Global Medical Affairs Leader - H&N CancerRaritan, New JerseyAnalytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Digital Culture, Digital Literacy, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, Process Optimization, Product Strategies, Stakeholder Analysis, Strategic Thinking . The sGMAL will partner closely with the GMA Operations Leader, Marketing and Market access leader, Regional Medical TA/product leaders and Clinical Development Leader to develop an integrated global medical affairs perspectives, strategies and plans.
Clinical Psychology Post Doctoral Fellow The Cass Center for Psychological and Holistic WellbeingClinical Psychology Post Doctoral FellowShort HIlls, NJRemoteFull timeIn this role, you will conduct psychological exams and testing, diagnose and treat psychological disorders, and assist patients in addressing dysfunctional behaviors. If you are an experienced Fellow passionate about providing high-quality care and mental health solutions, we want to hear from you!
NewClinical Director of Adult Autism Services (BCBA) JobotClinical Director of Adult Autism Services (BCBA)Paramus, NJ$110,000–$125,000 / year110K–$125K • Lead adult autism services • Shape day and community programs • Direct access to executive leadership • Build employment partnerships • Develop clinical leaders • Mission-driven ABA work . Its Adult Services Program supports adults across day and community-based settings, with individualized programming focused on employment, volunteering, functional life skills, recreation, social development, and long-term quality of life.
Clinical Supplies Manager SystimmuneClinical Supplies ManagerPrinceton, NJFull timeIt specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
Director, Global Clinical Physician (Cardiovascular) Bristol-Myers Squibb CoDirector, Global Clinical Physician (Cardiovascular)Princeton, NJ$275,630–$333,998 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. In collaboration with the Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets.
Veterinary Clinical Mentor, Emergency & Critical Care Ethos Veterinary HealthVeterinary Clinical Mentor, Emergency & Critical CareWest Caldwell, NJFull timeWith comprehensive services including 24/7 emergency care, advanced anesthesia, diagnostics and radiology, internal medicine, orthopedic and soft-tissue surgery, and radiation oncology, AERA stands at the forefront of specialty and emergency veterinary medicine—where advanced clinical expertise meets genuine compassion for patients, clients, and each other. We are proud recipients of the 2024 Neighborhood Fave award, recognized by Newsweek as one of America’s Best Animal Hospitals of 2025, and honored with the dvm360 Hospital Design Merit Award for our innovative, state-of-the-art facility.
Clinical Trial Manager KardiganClinical Trial ManagerPrinceton, New JerseyThis position will be responsible for the oversight and management of Clinical Research Organizations (CROs) and vendors and will work cross-functionally on the trial operations’ strategy and related initiatives. Supports the Clinical Trial Lead (CTL) in the oversight and management of study CROs to ensure that the study(ies) are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines.
Manager, Clinical Sciences Novartis AGManager, Clinical SciencesEast Hanover, NJLI HybridThe Manager, Clinical Sciences is responsible and accountable for execution of assigned clinical research tasks related to Investigator-Initiated Trials (IITs), Research Collaborations (RCs,) and Non-Interventional Studies / Local Interventional Studies (NIS/LIS).Manager, Clinical Sciences role is critical to support the growing complexity and volume of clinical studies (IITs & RC), evidence generation activities, and cross-functional collaborations. Establishes charters for and support management of Steering Committee (SC) and Executive Oversight (EO).Conducts Pre-Review Committee (RC) alignment and Ensure External Party Risk Management (EPRM) and Third-Party Impact Assessment Tool (TPIAT) completion for RCs (internal and external interface management).Responsible for the initial and subsequent drug supply across trials within a therapeutic area in collaboration with the Local Clinical Supply Manager.
NewClinical Supplies Manager Paramus, NJ ESRhealthcare and EXEC STAFF RECRUITERSClinical Supplies Manager Paramus, NJParamus, New JerseyReview manufacturing, packaging, and labeling Master and Executed Packaging Work Orders/Batch Records (MBR/EBR, Packaging Labeling Approval Forms (PLAF), Labeling Approval Forms (LAF), etc. Assist and support in writing and preparation of regulatory submission documents: drug product and drug substance sections in IND, Annual reports, and Informational amendments.
NewSenior Director, Clinical Development Acadia Pharmaceuticals IncSenior Director, Clinical DevelopmentPrinceton, NJ$306,100–$382,600 / yearWe are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. CNS clinical research experience is required, including demonstrable experience in successfully creating and implementing development plans and clinical studies; demonstrable experience in neurodegenerative and / or psychiatric disorders is preferred.
Clinical Document Migrations Manager Novartis AGClinical Document Migrations ManagerEast Hanover, NJ$49,140–$91,260 / yearEssential Requirements:Degree in information or life sciences/healthcare and extensive experience in Pharmaceuticals, Life sciences, and Clinical ResearchProven track record in leading of clinical document management, TMF and/or records & information management, with a deep knowledge of Trial Master File (TMF) reference model and experience in Electronic Document Management systems, specifically in Clinical and Regulatory (e.g. This role offers a unique opportunity to influence enterprise-wide digital transformation, working at the intersection of business and technology to drive migration initiatives with an objective of overall electronic Trial Master File (eTMF) system consolidation, TMF integration for Business Development & Licensing (BD&L) deals and TMF Document transfers ensuring compliance in collaboration with other CDGM groups, business and Information Technology (IT) departments.
Sr. Manager, Clinical Trial Lead KardiganSr. Manager, Clinical Trial LeadPrinceton, New JerseyMulti-dimensional Clinical Operations background with capability of devising plans for operational challenges such as site activation, subject enrollment, monitoring oversight, protocol deviation management, data cleaning, etc. The CTL may lead trials at a global level (overseeing multi-regional execution) or at a regional level (driving operational delivery in assigned countries/territories), depending on business needs.
Clinical Research Coordinator- Warren, NJ (Temp to Perm) The IMA GroupClinical Research Coordinator- Warren, NJ (Temp to Perm)Warren, New JerseyOur Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
Clinical Research Nurse Hackensack Meridian HealthClinical Research NurseParamus, New JerseyFull timeAssists 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.
Clinical Research Administrative Assistant Frontage Clinical Services IncClinical Research Administrative AssistantSecaucus, NJ$20–$22 / hourOur 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. Position Summary: We are seeking a proactive and detail-oriented Clinical Research Assistant to provide critical administrative and operational support within our research environment.
Clinical Research Director SanofiClinical Research DirectorMorristown, NJ$206,250–$343,750 / yearParticipates and contributes to regulatory and safety documents and discussions: Reviews and/or contributes clinical sections of the Investigator Brochure, IND/IMPD filings, DSUR, development risk management plans. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen.
Clinical Research Nurse Actalent IncClinical Research NurseParamus, NJ$54–$60 / hourThis role serves as a key liaison among principal investigators, sub-investigators, clinical research nurses, regulatory specialists, and study patients, supporting trial feasibility, regulatory submissions, patient recruitment and education, and accurate documentation of all study-related activities. Assist principal investigators in preparing proposed clinical trials by reviewing trial protocols, contacting departments that will provide study resources, and ensuring appropriate departments are notified and receive trial documentation, including scientific merit and accrual potential.
Senior Specialist, Clinical Data Management - Hybrid Merck & Co IncSenior Specialist, Clinical Data Management - HybridRahway, NJ$117,000–$184,200 / yearProject Management skills Ability to present in a group environment Leadership, verbal and written communication, interpersonal and organizational skills Desire and ability to learn new processes and technologies Broad knowledge of Clinical Development and Regulatory Affairs requirements Ability to multi-task, work independently, and good communication skills Understanding of drug discovery process, FDA regulations, GxP guidelines, ICH guidelines, clinical database cleaning process, and 21 CFR Part 11. Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc Fortrea IncFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncTrenton, NJRemote$125,000–$140,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
Sr. Principal Scientist, Clinical Operations Immunology Lead Merck & Co IncSr. Principal Scientist, Clinical Operations Immunology LeadRahway, NJ$210,400–$331,100 / yearIn a competitive external landscape and fast-paced internal environment, the Immunology Clinical Operations Lead position provides both strategic and operational leadership across early immunology programs, ensuring timely, high-quality execution of clinical studies and clinical pharmacology strategies worldwide. Translational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients.
Clinical Account Manager - New Jersey InSightec LtdClinical Account Manager - New JerseyNJThis role is responsible for supporting the long-term success of MRgFUS programs by fostering strong clinical relationships, helping our sites to optimize operational workflows, and aligning with institutional goals. We work together in a dynamic collaborative environment to deliver successfully while believing and driving a life-work balance philosophy that encourages our employees to do things that are meaningful outside of work.
Senior Manager, Data Engineer, Clinical Operations Bristol-Myers Squibb CoSenior Manager, Data Engineer, Clinical OperationsPrinceton, NJ$153,770–$186,327 / yearCollaborate with data product owners, engineers, and data scientists to develop and operationalize cloud-based GenAI and LLM-powered applications, utilizing techniques such as RAG, fine-tuning, and vector embeddings to deliver high-quality data discovery and consumption features for clinical operations workflows. Collaborate with BI&T partners, clinical study teams, Clinical trial analysts, trial managers, clinical operations leads, domain experts, and cross-functional leaders in data engineering, data product teams, and data operations to support effective adoption of our Data Platform.
NewClinical MD DO Geneticist Saint Peter's Healthcare SystemClinical MD DO GeneticistNew Brunswick, NJ$175,000–$750,000 / yearThe Department has been designated by the New Jersey State Department of Health as central Jersey's Regional Center for Newborn Screening and General Genetic Services and houses one of the largest comprehensive Lysosomal Disease Therapy Centers in the United States. Full-time compensation at Saint Peter's Healthcare System ranges from $175,000 - $750,000, which is impacted by various factors, including but not limited to physician specialty, years of experience, academic and administrative appointment, and pre-established metrics on productivity/patient engagement/quality.
Clinical Specialist - New Brunswick, NJ Procept Biorobotics CorpClinical Specialist - New Brunswick, NJNew Brunswick, NJIt continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept's history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do.
Clinical Dietitian I RWJ Barnabas Health Medical IncClinical Dietitian ILinden, NJ$73,427–$94,938 / yearPatient Safety Competencies: Monitors closely for high-risk food and drug interactions; ensures patients at nutritional risk receive timely assessments and adheres strictly to medical error/risk reporting protocols. Patient & Staff Education: Conducts structured in-service education programs for the renal staff regarding dialysis nutritional guidelines; coordinates and participates in initial education sessions and follow-ups for THRIVE patients.