Clinical Nutrition Manager III - Healthcare Sodexo SAClinical Nutrition Manager III - HealthcareEDISON, NJ$103,445–$133,870 / yearProvide executive leadership and strategic oversight for multi-site clinical nutrition and foodservice programs, ensuring alignment with client goals and organizational mission. In this leadership role you will oversee clinical nutrition and patient foodservice operations across multiple healthcare sites.
2027 Future Talent Program - Country Clinical Quality Manager US - Intern Merck & Co Inc2027 Future Talent Program - Country Clinical Quality Manager US - InternRahway, NJ$39,908–$111,111 / yearActivities may include (but are not limited to): Support the US CCQM team which oversees quality operations for trials conducted by GCTO US, Conduct data analysis for key CCQM activities to identify trends and/or process improvements needed, Develop tools to enhance support of audits, inspections as well as Quality Control and local training activities, Support benchmarking activities for quality deliverables, Develop presentations illustrating internship activities and deliverables. 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.
Global Director, Clinical Project Management Systimmune IncGlobal Director, Clinical Project ManagementPrinceton, NJ$180,000–$230,000 / yearIt specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
Senior Director, Global Clinical Project Management - Oncology Systimmune IncSenior Director, Global Clinical Project Management - OncologyPrinceton, NJ$210,000–$260,000 / yearAlongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).
Global Director, Clinical Project Management SystImmune, Inc.Global Director, Clinical Project ManagementPrinceton, NJ$180,000–$230,000 / yearIt specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
Regulatory & Clinical Affairs Manager PEAK Technical Services Inc.Regulatory & Clinical Affairs ManagerPrinceton, NJ$150,000–$185,000 / yearThis individual will prepare and execute FDA, EU MDR, and international regulatory submissions while partnering closely with engineering, quality, and clinical teams throughout product development. Experience supporting Software as a Medical Device (SaMD), AI/ML-enabled medical devices, medical imaging, digital health, robotics, or surgical navigation products.
2027 Future Talent Program - Global Clinical Trial Operations Epidemiology Operations - Intern Merck & Co Inc2027 Future Talent Program - Global Clinical Trial Operations Epidemiology Operations - InternRahway, NJ$39,908–$111,111 / yearThe intern will engage with the Epidemiology Operations organization and their associated project teams throughout participation in and/or leadership of initiatives that drive the efficient and ethical conduct of epidemiology trials across GCTO. Required Education: Candidates must be currently enrolled in a full-time BS/BA (or higher) degree program in a business or project management, continuous improvement, computer technology, or science related discipline.
Clinical Research Coordinator – Cardiovascular VitaliefClinical Research Coordinator – CardiovascularRahway, NJ$65,000–$80,000 / yearIMPORTANT 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.
Clinical Director, Oncology Early Development Merck & Co IncClinical Director, Oncology Early DevelopmentRahway, NJ$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Early Oncology therapeutic area.
Nurse Educator - Clinical Education - Trenton - Full-Time - DAYS Capital HealthNurse Educator - Clinical Education - Trenton - Full-Time - DAYSTrenton, NJ$86,528–$113,630.40 / yearRequires NIH Stroke Scale Certification (or must obtain by end of orientation) AND 8 hours of Stroke related Continuing Nursing Education (CNE) contact hours annually if assigned to: Critical Care, Intermediate Care Unit, Emergency Department, Neuro Units, Cardiology Inpatient at Hopewell, Peds ED, PACU, Interventional Radiology, CNI, Observation, Hospital at Home. CPR Requirements: Requires ACLS (or must obtain within 6 months of hire date) if assigned to: Critical Care/Intermediate/Telemetry, Emergency Rooms, Pediatrics/Pediatrics Emergency Room, Labor & Delivery, Surgical Services (not to include Perioperative), Interventional Procedures, Observation.
Sr.Clinical Data Manager Katalyst Healthcares & Life SciencesSr.Clinical Data ManagerEdison, NJPerform or provide oversight to staff for all CDM activities from study startup to archival: design CRFs/eCRFs, create Data Validation Specifications, Data Management Plans, eCRF Completion Guidelines, and Data Review Plans, code terms in MedDRA and WHO Drug; and complete data base lock, archival, and closeout activities. Expertise in development, validation, and management of the clinical study database throughout its life cycle, from CRF design, database development and testing, discrepancy management, data quality review and database close and lock procedures, CDASH and SDTM data formats.
Clinical Data Management Manager Integra LifeSciences Holdings Corp.Clinical Data Management ManagerPrinceton, NJ$109,250–$149,500 / yearUse procedural expertise and analytical skills to represent data management in cross-functional forums with clinical study teams, Biostatistics, Medical Affairs, and external partners to ensure effectiveness of data management deliverables such as database design, overall data quality, and data outputs for analysis. Tools And Equipment Used: Experience using Clinical Data Management systems, including Electronic Data Capture (EDC) and electronic Trial Master File (eTMF) platforms; Veeva CDMS and Veeva eTMF experience preferred.
Clinical Research Associate - Part Time Saint Peter's Healthcare System IncClinical Research Associate - Part TimeNew Brunswick, NJMaintain oversight of designated research project study activities including performing the following functions: Subject recruitment, Consenting and Enrollment/Randomization, Perform study procedures/assessments in accordance with clinical trial guidelines, Complete Data Entry into Case Report Forms and Query Resolution, Process/Ship Specimens per trial requirements, Maintain Regulatory files including delegation logs, FDA form 1572, training logs and other trial documents in compliance with federal and local regulations, Process IRB amendments, annual renewals, closures, etc, Attend regular meetings with members of the project at partnering institutions and sponsors to report on study progress. Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and updating the Informed Consent Form with CIRB Boilerplate, Completion of Institutional Review Board (IRB) modifications with supporting documentation.
Sr. Manager/Associate Director, Clinical Pharmacology Systimmune IncSr. Manager/Associate Director, Clinical PharmacologyPrinceton, NJ$150,000–$200,000 / yearThe ideal candidate will provide expertise in pharmacokinetics, dose optimization, pharmacometrics, and drug interaction assessment, collaborate with cross-functional teams (Clinical, Research, Regulatory, Biometrics, etc.), and manage clinical pharmacology studies, data analysis, and regulatory filings. Take a lead role in preparing and meticulously reviewing clinical pharmacology sections of study protocols, reports, investigators brochures and regulatory filings (IND's, BLA's, etc.), and responds to regulatory inquiries related to clinical pharmacology.
Clinical Nurse Education Specialist - Oncology - Per Diem Days Hackensack Meridian HealthClinical Nurse Education Specialist - Oncology - Per Diem DaysNeptune, New JerseyPer diemAs 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. 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.
NewPrincipal Scientist, Translational Clinical Biomarkers - Hematology/Oncology Merck & Co IncPrincipal Scientist, Translational Clinical Biomarkers - Hematology/OncologyRahway, NJ$190,800–$300,300 / yearRequired Skills: Biomarkers, Clinical Development, Clinical Research, Ethical Compliance, Immuno-Oncology, Mechanism of Action, Oncology, Patient Care, Pharmacodynamics, Protocol Development, Research Designs, Scientific Presentations, Scientific Writing, Strategic Thinking, Translational Medicine. For solid tumors, develop strategies addressing target expression, tumor biology, molecular subtype, immune contexture, circulating biomarkers, mechanisms of response and resistance, and potential predictive biomarkers.
Associate Director, Clinical Science Bristol Myers SquibbAssociate Director, Clinical SciencePrinceton, NJ$173,217–$209,899 / 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 Medical Writing and Clinical Operations, prepares study protocols, amendments, specific sections of study manuals and Investigator meeting materials, and other documents as needed with appropriate guidance and supervision.
Clinical Leader/Assistant Nurse Manager RN (ICU/CCU & Stepdown) - Nights CentraState Healthcare SystemClinical Leader/Assistant Nurse Manager RN (ICU/CCU & Stepdown) - NightsFreehold, New Jersey$107,250–$182,330 / yearFull timeDevelops new clinical pathways, monitors patient progress on current clinical pathways, reviews variances with Patient Care Reviewers, reviews variances from Quality Management with the Director/Nurse Manager and staff and reports to Nursing Quality Council. Both the CCU and Stepdown Unit benefit from strong operational support, including PCTs, dedicated Health Unit Coordinators, a Mobile Vascular Access Team for peripheral and central line procedures, and four Clinical Leaders who serve as readily available resources.
Clinical Trial Specialist Actalent IncClinical Trial SpecialistNew Brunswick, NJ$35–$38 / hourCoordinate the initiation and activation of new clinical trial protocols, ensuring all required approvals are in place before study activation, including Scientific Review Board, Institutional Review Board, Human Research Oversight Committee, data collection plans, and finance/contract approvals. This role ensures that all regulatory, ethical, and operational requirements are met, while working closely with research nurses, physicians, and study sponsors to deliver high-quality, compliant research that advances cancer care.
NewClinical Operations Manager GEE Group, IncClinical Operations ManagerPrinceton, NJ$101,000–$119,000 / yearThey will work in collaboration with the Operations Manager (in a dyad partnership) and Practice Managers at all locations and areas (eg: Stephen Klein Wellness Center/SKWC, Pathways, Hub of Hope, Mobile Medicine and Street Medicine) to develop and implement staff schedules to ensure adequate coverage and optimal patient care. Care Coordination: Serves as the primary care coordinator between the patient, other healthcare services areas (eg: dental, pharmacy), other services (eg: residential, case management) and other entities (eg: hospital connections, visiting nurse agency).