• Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of ... data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical trial billing… more
    SUNY Upstate Medical University (11/27/25)
    - Related Jobs
  • Senior Clinical Research

    Parexel (Albany, NY)
    **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned ... Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years relevant experience in … more
    Parexel (12/07/25)
    - Related Jobs
  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... monitoring patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval letters and annual review… more
    SUNY Upstate Medical University (12/01/25)
    - Related Jobs
  • Clinical Research Associate 2

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: The Clinical Research Associate II (CRA II)will join a team of experienced coordinators and manage various research trials, including first ... with clinical documentation and HIPAA guidelines is required. Preferred Qualifications: Clinical Research Associate Certification (SOCRA or ACRP) OR… more
    SUNY Upstate Medical University (01/01/26)
    - Related Jobs
  • Clinical Research Associate

    IQVIA (New York, NY)
    …bring breakthrough treatments to patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play ... Your work will directly contribute to the integrity and quality of clinical research data. **Key Responsibilities** + Conduct all types of site visits-selection,… more
    IQVIA (01/05/26)
    - Related Jobs
  • Sr. Clinical Research

    Parexel (Albany, NY)
    …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery ... associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of… more
    Parexel (12/10/25)
    - Related Jobs
  • Sr. Clinical Research

    Parexel (Albany, NY)
    The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) + Preferred… more
    Parexel (12/11/25)
    - Related Jobs
  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: The Clinical Research Associate I (CRA I) will join a team of experienced associates and manage various research trials, including first in ... I will interact daily with clinicians, sponsors, IRB, regulatory agencies and other research professionals. This is a subject / patient facing role, the candidate… more
    SUNY Upstate Medical University (12/09/25)
    - Related Jobs
  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    Job Summary: This position is responsible for the coordination of ALS clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO ... data collection and entry into paper and electronic databases, maintenance of clinical research supply inventory, processing clinical trial billing… more
    SUNY Upstate Medical University (10/16/25)
    - Related Jobs
  • Clinical Research Associate

    Touro University (Hawthorne, NY)
    …adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities ... with clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research . + Monitor study patients for adverse events in… more
    Touro University (10/23/25)
    - Related Jobs