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Clinical Operations Jobs in Neptune, NJ

This full-time position is responsible for ensuring the integrity, quality, and compliance of clinical trials conducted at Astera Cancer Care.

Job Description:.

Rahway, NJ8 days ago
  • $173,200–$272,600 Per Year

p>Enterprise Leadership Skills:

  • Business Savviness | Uses organizational and industry insights to identify trends, assesses Data Management operating practices and performance, evaluates process or operating model changes, and anticipates impacts on delivery, resourcing, and stakeholders. The role proactively engages with stakeholders across GDMS and Global Clinical Trial Operations (GCTO) to ensure aligned intake, business case and resource evaluation, approval, leadership assignment, execution oversight, implementation, and value realization.

New Brunswick, NJ30+ days ago
  • $139,570–$169,126 Per Year

p>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.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.

New Brunswick, NJ30+ days ago

Aligned with Rutgers University-New Brunswick and collaborating university wide, Rutgers Health 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.

New Brunswick, NJ30+ days ago

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.

East Brunswick, NJ29 days ago
  • $80,000–$100,000 Per Year

Essential Competencies: Strong communication skills, including the ability to communicate effectively in both written and verbal forms with all levels of practice employees and stakeholders, as well as peers and leadership within the OneOncology IT and service desk team. OneOncology is positioning community oncologists to drive the future of medical care through a patient-centric, physician-driven, and technology-powered model to help improve the lives of everyone living with cancer and other diseases.

East Brunswick, NJ30+ days ago
  • $140,000–$190,000 Per Year

This leader owns the end-to-end experience strategy, execution, and cross-functional integration that bring each brand's vision to life, reinforcing Solta's premium positioning across Thermage, Fraxel, Clear + Brilliant, and VASER. Partner with Brand Managers to translate brand strategies and messaging frameworks into cohesive, high-impact event experiences that achieve commercial and customer engagement goals.

Somerset, NJ30+ days ago
  • $110,706–$145,303 Per Year

Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. The successful candidate will translate clinical and CMC needs into executable supply plans, ensure compliant distribution, inventory control, and QP release, and partner cross functionally to enable uninterrupted delivery of product to global clinical sites.

NJ30+ days ago

Monitor and review study budget and data management activities, such as PRF development, training, and facilitating query resolution with proper documentation • Support monitoring efforts by setting quality and compliance goals by overseeing and approving study monitoring plans, may review, suggest edits and approve monitoring trip reports • Contribute to contract review and negotiations with outside vendors and study sites or laboratories • Mentor CTMs and CRAs • Demonstrate an ability to influence others to achieve positive results and collaboration through diplomacy and respect for others, appropriate prioritization and facilitation of the decision-making process Qualifications Qualifications: • Bachelors degree or higher, or equivalent credentials • Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements • Strong interpersonal skills (verbal and written), organizational, and prioritization skills, able to communicate at multiple levels of an organization and with sponsors/clients. Primary Responsibilities (all levels): • Manage, design and implement all clinical operational aspects of IVD clinical trials from inception through close-out • Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings • Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and/or vendor management for the study, where applicable • Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials • Ensure trial master file (TMF/eTMF) is established, current, and maintained per ICH E6.

Colgate-Palmolive Co logo

Piscataway, NJ28 days ago
  • $250,000–$275,000 Per 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.

    • Toms River, New Jersey30+ days ago

    Additionally, they maintain accurate records related to the staffing and delivery of service for each case as well as assist in the creation, maintenance, and management of a master schedule, adequately staffing clinical cases according to the budgeted hours per client as authorized by the client's insurer. Company: Kaleidoscope Family Solutions ABA, IncContract Contact: HQ CareersOffice Email: Recruit@kfsaba.orgOffice Phone: 877-ABA-0399Office Address: 950 E Haverford Road, Suite 100A, Bryn Mawr, PA 19010.

    East Brunswick, New Jersey30+ days ago

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    OneOncology is positioning community oncologists to drive the future of medical care through a patient-centric, physician-driven, and technology-powered model to help improve the lives of everyone living with cancer and other diseases.

    • Strong communication skills, including the ability to communicate effectively in both written and verbal forms with all levels of practice employees and stakeholders, as well as peers and leadership within the OneOncology IT and service desk team.

    Somerset, NJ30+ days ago
    • $127,313–$167,099 Per Year

    Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. Director of Clinical Operations and collaborates with Clinical Operations, Data Management, QA, ITQA, central labs, specialty labs, CROs, sites, and other cross-functional stakeholders.

    Colgate-Palmolive Company logo

    Piscataway, NJ29 days ago
    • $250,000–$275,000 Per Year

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

    NJ30+ 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.

    NJ30+ days ago

    LifeStance is a national provider of mental healthcare services focused on evidenced-based, medically driven treatment services for children, adolescents and adults suffering from a variety of mental health issues in an outpatient care setting, both in-person at its 550+ clinics nationwide and through its digital health telemedicine offering. Additionally, this position identifies and develops strategic growth opportunities, monitors regional performance, and works closely with corporate and shared services teams to develop competitive strategies in alignment with LFST's mission and values.

    South Plainfield, NJ30+ days ago
    • $92,000–$145,000 Per Year

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    Minimum of one year experience required in management (healthcare, business, or military) or equivalent renal experience (nurse, dietitian, social worker, LPN, etc.) at discretion of DVP and/or ROD.

    The Hospital Services Administrator is responsible for overseeing the administration and coordination of services to licensed Acute and Sub-Acute Care Programs in the Hospital Services Group.

    NJ25 days ago
    • $86,000–$94,000 Per Year

    For information on job scams, visit, https://www.consumer.ftc.gov/JobScams or file a complaint at https://www.ftccomplaintassistant.gov/.

    Our primary, multispecialty, and urgent care providers serve millions of patients in traditional practices, patients' homes and virtually through VillageMD and our operating companies Village Medical, Village Medical at Home, Summit Health, CityMD, and Starling Physicians.

    New Brunswick, NJ8 days ago
    • $132,300–$160,320 Per Year

    Position Summary: The Senior Manager, Capital Services & Solutions (CS&S) Operations is responsible for driving operational excellence across the entire CS&S organization through strategic planning, operational coordination, executive reporting, budget oversight, workforce planning support, leadership support, and continuous improvement initiatives. Capital Services & Solutions Overview: Our Capital Services & Solutions pillar within the Global Technical Services business unit is responsible for the safe, sustainable, and cost-effective construction, operation and maintenance of world-class facilities that enable the discovery, development and delivery of innovative medicines that help patients prevail over serious diseases.

    Summit West, NJ30+ days ago
    • $103,560–$125,495 Per Year

    Is required to perform Cell Therapy manufacturing to maintain hands on expert knowledge of each Unit Operation, demonstrate what good execution looks like to new WCT members and when necessary, back fills for absent team members or makes up the execution resource requirements to meet the production schedule. Is responsible to provide the Production Scheduling team with information (daily, weekly monthly) on the availability of their WCT production resources and tracks/maintain records of all team members actual availability vs planned or unplanned absence due to holidays, sickness or other reasons.

    NJ30+ days ago

    Working knowledge of MS Office suite and MS Project or equivalentl Strong communication and presentation skillsl In-depth knowledge of applicable clinical research trails regulatory requirement (i.eGCP and ICH guideline) Competencies: 1 Solid problem solving andtime management skills2 Excellent verbal and written skills3 Great interpersonal skills4 Strong attention to detail5 Highly organized6 Ownership and result driven. Manage CRO and site budgets, communicate deviations from budget projections, and propose solutions for budget deviations.l Support with cross-functional team to facilitate the trial protocol development and maintenance process.l Collaborate with supply Chain team to develop and complete of the request and management for Clinical Supplies.l Provide input to process development and improvement.l

    New Brunswick, NJ30+ days ago
    • $94,180–$114,124 Per Year

    p>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.

    If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.

    Rahway, NJ30+ days ago
    • $45,900–$72,200 Per Year

    p>Required Skills:

    Chemical Plant Operations, Chemical Plant Operations, Cleanroom Gowning, Clinical Development, CNC Operations, Computer Literacy, Conventional Machining, Detail-Oriented, Drilling Machines, Electronic Systems, Equipment Set Up, GMP Compliance, Good Manufacturing Practices (GMP), Manufacturing Processes, Material Selection, Microsoft Word, Oral Communications, Preventive Action, Process Improvements, Production Scheduling, Quality Initiatives, Quality Monitoring, Safety Procedures, Shift Work, Systems Troubleshooting {+ 1 more}.

    Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms.

    Neptune, New Jersey22 days ago

    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.

    • Rahway, NJ8 days ago
    • $173,200–$272,600 Per Year

    p>Enterprise Leadership Skills:

    • Business Savviness | Uses organizational and industry insights to identify trends, assess Data Management operating practices and performance, evaluate process or operating model changes, and anticipate impacts on delivery, resourcing, and stakeholders.

    • Partners with GDMS functional area heads and Business Operations leadership to evaluate and characterize adoption, performance, and value realization risks and develop targeted change management strategies to drive enhanced business readiness and adoption success.

    Rahway, NJ24 days ago
    • $63,800–$100,400 Per Year

    p>Required Skills:

    Biopharmaceutical Manufacturing, CNC Operations, Computer Literacy, Data Analysis, FDA Regulations, Good Manufacturing Practices (GMP), Laboratory Techniques, Manufacturing Quality Control, Master Batch Records, Material Selection, Pharmaceutical Process Development, Production Planning, Regulatory Compliance, Shift Work, Teamwork.

    This position will be responsible for hands-on processing activities that include equipment assembly and disassembly, sterile processing, inventory management, open aseptic formulation in an isolator and closed formulation activities in a Grade C environment, and manual visual inspection of filled units (i.e. vials or syringes).There is also opportunity to cross-train in other areas, such as filling.

    Rahway, NJ21 days ago
    • $52,500–$82,700 Per Year

    p>Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms.

  • Experience with some of the following: highly complex and state of the art equipment, isolators, containment technology, aseptic filling using automated machinery, sterile manufacturing, visual inspection of product in glass vials, SAP or other ERP systems.

    • Rahway, NJ24 days ago
    • $50,700–$79,900 Per Year

    p>Required Skills:

    Adverse Event Reporting System, Adverse Event Reporting System, Autoclaving, Buffer Preparation, Clinical Development, Detail-Oriented, Drug Development, Electronic Systems, Fermentation Process Development, Fermentation Tanks, Filtering Equipment, GMP Compliance, Good Manufacturing Practices (GMP), Liquid Chromatography (LC), Machinery Operation, Manufacturing Documentation, Manufacturing Processes, Media Preparation, Microsoft Office, Preventive Action, Process Control, Production Scheduling, Purification Methods, Raw Photo Workflow, Safety Practices {+ 1 more}.

    Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms.

    New!

    Rahway, NJ5 days ago
    • $68,000–$107,000 Per Year

    p>Required Skills:

    Applied Research, Applied Research, Biopharmaceutical Manufacturing, CNC Operations, Computer Literacy, Data Analysis, Enterprise Resource Planning (ERP), Enterprise Resource Planning (ERP) Systems, FDA Regulations, GMP Compliance, Good Manufacturing Practices (GMP), Laboratory Techniques, Manufacturing Quality Control, Manufacturing Support, Master Batch Records, Material Selection, Pharmaceutical Process Development, Preventive Action, Production Planning, Regulatory Compliance, Safety Protocols, SAP Enterprise Resource Planning (ERP), SAP Systems, Shift Work, Sterile Procedures {+ 1 more}.

    Pharmaceutical Operations and Clinical Supply is seeking highly motivated individuals for R&D Operations roles in our Rahway, NJ, Formulation, Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms.

    NJ30+ days ago
    • $35–$47 Per Hour

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  • Minimum level of education and years of relevant work experience:
  • Bachelor's degree in a relevant life science or healthcare-related discipline and minimum 2 years of clinical research support experience in a pharmaceutical, biotechnology, or related environment or a recognized equivalent of education and experience. This involves supporting Clinical Trial Managers (CTMs) with activities related to:

    study start-up investigator site feasibility and selection essential document review related to investigator site initiation and investigational product release and patient enrollment.

    • New!

    New jersey City, NJ4 days ago

    ul>

  • Define the canonical data model for Manufacturing and Operations entities such as material, BOM, routing, work order, production order, inventory, warehouse, plant, machine, capacity, and quality records. We are seeking a Manufacturing Operations Data Domain Lead to define the canonical data model for manufacturing and operations data across SAP, PeopleSoft, and the datalake ecosystem.

    • NJ30+ days ago

    p>The Project Manager, Clinical Trials develops and implements comprehensive workflows and project/patient tracking procedures and tools to ensure ongoing clinical trial compliance across the assigned Research Program or Division.

    In addition, this role will be responsible for coordinating all aspects of clinical trial feasibility, start-up, conduct and close-out of all Clinical Trials being conducted within their assigned Research Program or Division.

    Rahway, NJ30+ days ago
    • $255,800–$402,700 Per Year

    The Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.

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