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Research Leader Jobs in Edison, NJ

BROOKFIELD PLACE FKA 3 WORLD FINANCIAL CENTER, 200 VESEY STREET:NEW YORK

City:.

United States of America

Work hours/week:.

New York, NY30+ days ago
  • $100,000–$150,000 Per Year

With roots tracing back to 1881, the Company is engaged in a broad range of activities in the financial services industry, including retail securities brokerage, institutional sales and trading, investment banking (both corporate and public finance), equity & fixed income research, market making, trust services and investment advisory and asset management services. This salary range is specific to the City of New York and takes into account the wide range of factors that are considered in making salary decisions including but not limited to your skills, qualifications, experience, licensure and certifications, and other business and organizational needs.

New York, NY30+ days ago

With roots tracing back to 1881, the Company is engaged in a broad range of activities in the financial services industry, including retail securities brokerage, institutional sales and trading, investment banking (both corporate and public finance), equity & fixed income research, market making, trust services and investment advisory and asset management services. This salary range is specific to the City of New York and takes into account the wide range of factors that are considered in making salary decisions including but not limited to your skills, qualifications, experience, licensure and certifications, and other business and organizational needs.

Princeton, NJ30+ days ago

The role encompasses a broad range of expertise areas, including artificial intelligence, computer science, machine learning, human-computer interaction, educational data mining, learning analytics, and psychometrics. 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.

Parsippany, NJ28 days 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.

NY25 days ago
  • $60,000–$70,000 Per Year

Over the past year, Circuit has remained committed to breaking the norms that have challenged research participation and continues to extend reach within the research industry, having expanded client relationships with multiple pharmaceutical companies and contract research organizations. Circuit's accolades continued beyond the early years as a research industry watchlist company, including winning SCOPE's Participant Engagement Award in 2022 while continuing to receive national recognition as Fast Company's World Changing Ideas Award 2022.

New York City, NY18 days ago
  • $85,000–$90,000 Per Year

li>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.

    • IQVIA logo

    Parsippany, California30+ days ago

    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.

    IQVIA logo

    Parsippany, Pennsylvania30+ days ago

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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).

    IQVIA logo

    Parsippany, Pennsylvania30+ days ago

    div>

    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).

    IQVIA logo

    Parsippany, South Dakota10 days ago

    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.

    Hackensack, New Jersey11 days ago

    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.

    Hackensack, New Jersey30+ 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.

      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.

    Hackensack, New Jersey30+ days ago

    li>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. Responsibilities:

    A day in the life of a Senior Research Contract Specialist at Hackensack Meridian Health includes:

    • Provides services to investigators conducting Clinical trials at Hackensack Meridian Health.

    IQVIA logo

    Parsippany, Texas10 days ago

    Experience in cardiovascular studies and hands‑on familiarity with EDC entry, query resolution, prescreening referrals, reviewing charts from site databases, and related clinical research tasks are highly valued.

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

    NY7 days ago
    • $180,000–$200,000 Per Year

    ul>

  • Candidates located in higher-cost labor markets, including California, Washington, New York, New Jersey, Connecticut, Massachusetts, and Washington, DC represent the middle to high end of the range, while candidates located in all other U.S. locations represent the low to middle end of the range.
  • Maintain vendor relationships and work with Procurement to continuously streamline and improve the ability of business teams to gain insights from customers, physicians, patients, and other healthcare system stakeholders as required.

    • Sanofi logo

    Morristown, NJ7 days ago
    • $232,500–$335,833.33 Per Year

    li>

    Responsible for ongoing alignment of processes, objectives and improved ways of working for all aspects linked to patient/ caregiver generated data (eg, across health value translation as it relates to developing and delivering on the patient disease strategy, CSO for ePRO and digital health tech/ digital biomarkers; clinical sub teams for early alignment on differentiated COA strategy, etc).

  • Accountable for maintaining cross functional leadership connectivity within PDMD and beyond; Promote and facilitate cross-functional collaboration with internal biostats, translational medicine leadership, clinical research directors, global project heads and Health Economics and Value Assessment team members, global regulatory affairs, medical affairs.

    • Rahway, NJ15 days ago
    • $190,800–$300,300 Per Year

    li>Under the guidance of a senior leader, this position supports value evidence outcomes research plans and real-world evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment (HTA)/reimbursement agencies and health systems globally.

  • Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, health-care resource utilization and costs, physician and patient satisfaction surveys, clinical and patient- reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.

    • Rahway, NJ20 days ago
    • $255,800–$402,700 Per Year

    p>Required Skills:

    Cross-Functional Leadership, Early Drug Development, Evidence Generation, Executive Leadership, Global Experience, Health Services Research, Life Cycle Management, Outcomes Research, Patient Access, Payer Evidence, Payer Reimbursement, Pediatric Medicine, Real World Evidence (RWE), Vaccine Development, Vaccine Management.

    Under the guidance of a senior leader, this position leads a team of outcomes research professionals to develop value evidence strategies and generate real-world and economic evidence for a portfolio of products to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment (HTA)/ reimbursement agencies, and health systems globally.

    NY29 days ago
    Remote
    • $66,000–$94,000 Per Year

    Our Real-World Evidence team is hiring an Associate Research Scientist to join our team of research professionals conducting real-world studies in the pharmaceutical and biotech space, operating as a thought leader, problem solver, and data expert. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.

    Sanofi logo

    Morristown, NJ30+ days ago
    • $133.50–$192.83 Per Hour

    We are looking for a passionate, driven Digital Product Owner to join the Data Visualization & Decision Support product line within the In-Silico Research team, taking ownership of a critical digital product that empowers scientists to make faster, more confident, data-driven decisions. As Product Owner, you will own end-to-end delivery of one or more data visualization and decision support products, working in agile cross-functional pods alongside data scientists, ML engineers, UX/UI designers, and front-end developers.

    Rahway, NJ30+ days ago
    • $282,200–$444,200 Per Year

    Through clinical trials we ensure that our existing and pipeline products are developed to produce safe, effective, and innovative medicines, and we work with cross-functional colleagues in Global Medical and Scientific Affairs and Global Policy to ensure timely access to our medicines. Establishing communications with prominent clinical investigators in their particular field of interest, particularly those scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs.

    Rahway, NJ30+ days ago
    • $87,300–$137,400 Per Year

    Required Skills: Aseptic Technique, Aseptic Technique, Bioanalytical Techniques, Biomanufacturing, Bioreactor Operation, Cell Culture Process Development, Cell Cultures, Conducting Experiments, Cross-Functional Teamwork, GMP Compliance, High Throughput Screening HTS Systems, Mammalian Cell, Mammalian Cell Culture, Manufacturing Processes, Microbial Fermentation, Molecular Biology, Optimism, Process Optimization, Process Scale Up, Process Scheduling, Product Development, Protein Expression, Protein Purifications, Technical Leadership, Technical Transfer {+ 2 more}. MINIMUM EDUCATION REQUIREMENTS: Education: Bachelor's Degree with 2+ years of relevant experience or master's degree in chemical/Biochemical/Biomedical Engineering, Biotechnology, Biochemistry, Molecular Biology, or related fields with research background in molecular biology, cell culture or protein purification.

    Hackensack, New Jersey7 days ago

    Qualifications:

    Education, Knowledge, Skills and Abilities Required:

    • Bachelor`s Degree in Accounting, Sciences or equivalent experience and High School diploma, general equivalency diploma (GED), GED equivalent programs, and/or other Vocational degrees/certificates. 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.

    IQVIA logo

    Parsippany, Kansas17 days ago

    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.

    IQVIA logo
    New!

    Parsippany, New Mexico3 days ago

    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.

    New!

    New York, NY2 days ago
    • $180,000–$200,000 Per Year

    p>We are seeking a Senior Director, Research & Insights to lead a market-facing insights function that drives revenue, strengthens client partnerships, and advances the company's leadership position across digital advertising. The ideal candidate brings a strong commercial mindset and understands how research and insights directly drive product adoption, pipeline growth, client strategy, and measurable business outcomes.

    Sanofi logo

    Morristown, NJ30 days ago
    • $206,250–$343,750 Per Year

    p>The Clinical Research Director (CRD), Immunology and Inflammation Therapeutic Area, Solid Organ Transplant focus, is responsible for the development, execution and reporting of clinical trials in support of the registration of a product, directly reporting to the Clinical Lead in charge of the clinical strategy. In addition, the CRD is responsible for the development of abbreviated protocol and clinical protocol, participates to the review process for protocols, study reports, labeling, and contributes/supports interactions with regulatory agencies and ethics committees.

    Sanofi logo

    Morristown, NJ30+ days ago
    • $206,250–$297,916.66 Per Year

    p>In addition, the CRD is responsible for the development of abbreviated protocol and clinical protocol, participates to the review process for protocols, study reports, labeling, and contributes/supports interactions with regulatory agencies and ethics committees.

    The role requires a self-starting, creative, well-organized, strategic focused, resourceful individual with excellent emotional intelligence, self-motivation, solid analytical skills and the ability to deliver on multiple operational tasks.

    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.

    Princeton, NJ30+ days ago

    Provide scientific and technical skills so as to contribute to conceptualizing, designing, obtaining support for, conducting, and managing one or more of the following: (1) research projects or (2) development projects, particularly those for which scientific principles are applied to the creation of tools to improve the efficiency or quality of the practice of test development or statistical analysis; new item types; (3) the scoring of responses to open-ended items; (4) innovative assessment prototypes or products. Participate in dissemination activities through the publications of research papers in peer review journals and in the ETS Research Report series, the issuing of progress and technical reports, the presentation of seminars at major conferences and at ETS, or the use of other appropriate communication vehicles, including books and chapters, that impact practice in the field or at ETS.

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