• Organon & Co. (Jersey City, NJ)
    **Job Description** **The** **Position** The Clinical Trial Manager (CTM), Translational Medicine and Early Development (TMED) is responsible for assisting in ... vendors. The CTM will also assist to manage the clinical study team and help to coordinate meetings and...defining, monitoring and reporting on all aspects of key trial performance indicators, including for example, country and site… more
    DirectEmployers Association (10/23/25)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (Rahway, NJ)
    …Skills: Accountability, Accountability, Adaptability, Change Management, Clinical Development, Clinical Research, Clinical Trial Management, Clinical ... direction from the Director/Associate Director Publication Management, the Sr. Specialist Publication Manager coordinates publication planning and implementation, tracks… more
    HireLifeScience (11/14/25)
    - Save Job - Related Jobs - Block Source
  • Merck & Co. (Rahway, NJ)
    …- Primary activities include, but are not limited to: - Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area ... etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and...prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. - Responsible… more
    HireLifeScience (10/22/25)
    - Save Job - Related Jobs - Block Source
  • Principal Financial Group (New York, NY)
    …detailed proprietary analysis of therapeutics companies globally leveraging: + comprehensive clinical pipeline, trial data, commercial forecasting / competitive ... quantitative insights + Partner closely with Healthcare sector team leads, senior therapeutics analysts, and portfolio managers to provide outperformance through… more
    DirectEmployers Association (11/08/25)
    - Save Job - Related Jobs - Block Source
  • Sr. Specialist , Project Management…

    Merck (Rahway, NJ)
    …​ **Primary activities include, but are not limited to:** - Participates on the Clinical Trial Team (CTT) and collaborates closely with other functional area ... etc.) as well as other organizations such as Global Clinical Trial Operations (GCTO) Regional colleagues and...prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. - Responsible… more
    Merck (10/23/25)
    - Save Job - Related Jobs - Block Source
  • Senior Specialist , Publications…

    Merck (Rahway, NJ)
    …Skills:** Accountability, Accountability, Adaptability, Change Management, Clinical Development, Clinical Research, Clinical Trial Management, ... direction from the Director/Associate Director Publication Management, the Sr. Specialist Publication Manager coordinates publication planning and implementation, tracks… more
    Merck (11/15/25)
    - Save Job - Related Jobs - Block Source
  • Associate Director, Quality Risk Specialist

    Bristol Myers Squibb (Madison, NJ)
    …effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and establish a feedback loop to ... adjusted when new or unanticipated issues arise once the trial has begun. **Key Responsibilities:** + Develop the Quality...with the CAPA CoE and Serious Breach pillar and Clinical Quality Assurance to gather input from audits, inspections,… more
    Bristol Myers Squibb (10/30/25)
    - Save Job - Related Jobs - Block Source
  • Health System Specialist - Compliance…

    Veterans Affairs, Veterans Health Administration (East Orange, NJ)
    …care system. Analyzing and prioritizing local risks by working closely with senior management to develop a proactive strategy to mitigate compliance risks. Performs ... is not a virtual position. Position Description/PD#: Health System Specialist - Compliance Officer/PD99467S Relocation/Recruitment Incentives: Not Authorized Requirements… more
    Veterans Affairs, Veterans Health Administration (11/15/25)
    - Save Job - Related Jobs - Block Source
  • Clinical Research Coordinator

    Hackensack Meridian Health (Hackensack, NJ)
    …of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Education, Knowledge, Skills and… more
    Hackensack Meridian Health (11/13/25)
    - Save Job - Related Jobs - Block Source
  • Associate Director-Principal Medical Writer

    Sanofi Group (Morristown, NJ)
    …progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team (CTT) and Project Team. This is a position for a ... senior medical writer who has an extensive experience with the preparation of clinical documents and regulatory dossiers and has demonstrated leadership skills as… more
    Sanofi Group (09/06/25)
    - Save Job - Related Jobs - Block Source