• Study Associate I, Clinical

    Taiho Oncology (Princeton, NJ)
    …+ Coordinates cross functional study team meetings and supports study manager with meeting minutes for assigned studies . + Updates internal study ... it most. This is an exciting opportunity to support clinical studies and experience multiple facets of...Study Associate (SA) I is responsible for operational study support during study start -up,… more
    Taiho Oncology (07/03/24)
    - Save Job - Related Jobs - Block Source
  • Study Manager , Clin Operations,…

    Merck (North Wales, PA)
    …progressive on-the-job training and operational project assignments under the direction of Lead Clinical Scientist and Lead Study Manager . **Your Fellowship ... if you are among the intellectually curious, join us-and start making your impact today. **Overview:** Global Clinical...for a single study or across multiple studies (eg, operational deliverables, clinical & ancillary… more
    Merck (06/19/24)
    - Save Job - Related Jobs - Block Source
  • Manager , Site Contract Management…

    J&J Family of Companies (Trenton, NJ)
    Manager , Site Contract Management Start Up -...Establish and maintain methods to initiate study start up planning + Use knowledge of clinical ... 2406197284W **Description** Johnson & Johnson is recruiting for a ** Manager , Site Contract Management Start Up** to...function as a subject matter expert on GCO CCS study start up activities, specifically related to… more
    J&J Family of Companies (07/03/24)
    - Save Job - Related Jobs - Block Source
  • Senior Manager , Clinical Data…

    Bristol Myers Squibb (Princeton, NJ)
    …integrity & completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database Lock . **Position Summary:** ... The Senior Manager , Clinical Data Management is a leadership...not limited to:** Project Management and Leadership * Provides clinical data management leadership within the study more
    Bristol Myers Squibb (07/01/24)
    - Save Job - Related Jobs - Block Source
  • Director Clinical Research

    System One (Princeton, NJ)
    …(CDP). + Provide all necessary leadership and guidance to keep the quality of clinical study -related documents ( clinical study protocol (PRT), ... investigator's brochure (IB), clinical study report (CSR), medical monitoring plan (MMP), safety management...Minimum 10 years of experience in planning/developing, and managing clinical studies within the pharmaceutical industry. +… more
    System One (05/13/24)
    - Save Job - Related Jobs - Block Source
  • Clinical Scientist, Clin Operations,…

    Merck (North Wales, PA)
    …Lead Clinical Scientist and study team with the scientific conduct of clinical studies . In this position, you will have the opportunity to develop your ... for specific clinical /scientific activities on a single study or across multiple studies (eg, medical...and operational project assignments under the direction of Lead Clinical Scientist and Lead Study Manager more
    Merck (06/19/24)
    - Save Job - Related Jobs - Block Source
  • Clinical Data Manager Fellowship…

    Merck (North Wales, PA)
    …and external stakeholders ( study sites, vendors, committees, etc.) in support of clinical study objectives. You will be part of a diverse, cross-functional ... if you are among the intellectually curious, join us-and start making your impact today. **Overview:** Global Clinical...activities with the support and oversight of a Senior Clinical Data Manager (SCDM)/Lead Clinical more
    Merck (06/19/24)
    - Save Job - Related Jobs - Block Source
  • Clinical Trial Associate

    Bristol Myers Squibb (Princeton, NJ)
    …Internal: Global Trial Manager (GTM), Clinical Trial Managers (CTMs) Clinical Trial Monitors (CTMos), Study Start -up Specialists, Site Contract ... key internal matrix relationships and key external stakeholders/clients + External: Clinical Study Sites, Institutional Review Boards/Ethics Committees, Vendors,… more
    Bristol Myers Squibb (07/04/24)
    - Save Job - Related Jobs - Block Source
  • Clinical Supplies Project Manager

    Merck (West Point, PA)
    …in-house, 400+ outsourced or run by partners, and 300+ company Investigator Initiated Studies (IIS) clinical trials. GCS is accountable for the planning, ... evolving, so if you are among the intellectually curious, join us-and start making your impact today. **Overview:** Merck Research Lab's (MRL) Pharmaceutical… more
    Merck (06/19/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director Clinical Scientist,…

    Merck (North Wales, PA)
    …with the Medical Writer on clinical /scientific and regulatory documents. + Partners with Study Manager on study deliverables. + Participates in the set ... drives scientific planning, strategy and execution of Phase 1-4 clinical studies . Under the direction of the...up and design during study start up (eg, database set up)… more
    Merck (07/03/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director, Biostatistics

    Bristol Myers Squibb (Princeton, NJ)
    …trial design, analysis planning, study results presentation and interpretation, clinical study report authoring, regulatory submissions and publications. + ... manager , data manager , PK scientist, and other members of the study /indication team. **Primary Responsibilities** + Core member of an EDT and key sub-teams.… more
    Bristol Myers Squibb (05/26/24)
    - Save Job - Related Jobs - Block Source