• Study Associate I, Clinical

    Taiho Oncology (Princeton, NJ)
    operations practices and processes ensuring consistent delivery across studies . Education/Certification Requirements: + Associate 's degree or equivalent. ... impactful results. The leadership and support provided by our Clinical Operations team are the cornerstone of...dynamic team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for… more
    Taiho Oncology (11/13/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Trenton, NJ)
    …Trial Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations , the specialist ensures ... and system work instructions. Provide support and guidance to study team members during the full lifecycle of the...ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure… more
    Sumitomo Pharma (11/05/25)
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  • Associate Director, Clinical Science

    Bristol Myers Squibb (Princeton, NJ)
    …aspects of study design. + In collaboration with Medical Writing and Clinical Operations , prepares study protocols, amendments, specific sections of ... to, collaboration on functional area activities during program implementation, clinical study start-up/execution/close out, data analysis/reporting, and… more
    Bristol Myers Squibb (12/23/25)
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  • Senior Clinical Research Associate

    Parexel (Trenton, NJ)
    …or Director of Site Management and Monitoring (DSMM) + Partners with SCP and Country Study Operations Manager (SOM) + When required Partners with other Study ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is...Demonstrated knowledge in disease and technical areas pertaining to clinical studies , including knowledge of company direction,… more
    Parexel (12/07/25)
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  • Associate Medical Director, Clinical

    Sumitomo Pharma (Trenton, NJ)
    …director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators ... highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology**...and study staff. + Responsible for leading clinical study teams, monitoring overall study more
    Sumitomo Pharma (11/15/25)
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  • Associate Director, Clinical Trial…

    Vitalief (New Brunswick, NJ)
    …performance and trial outcomes. + Innovation-Driven: Operate at the intersection of clinical research, financial operations , and advanced technology to transform ... thought leadership forums. Required Qualifications: + 8+ years of experience in clinical research operations , financial management, or related roles. +… more
    Vitalief (12/30/25)
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  • Associate Director, TAIP Principal Analyst…

    Bristol Myers Squibb (Princeton, NJ)
    …analytics. This is an ideal opportunity for professionals with backgrounds in consulting, clinical operations , or trial analytics who are ready to take ownership ... of delivery and help shape the success of global studies . **Key Responsibilities** + Own study -level analytics...scoring, and performance dashboards + Engage directly with cross-functional study team members ( clinical , feasibility, ops, TA… more
    Bristol Myers Squibb (12/19/25)
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  • Associate Director, Statistics

    AbbVie (Florham Park, NJ)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Statistics provides statistical leadership for clinical ... of methodologies for confounding control and bias minimization in observational studies preferred. Key Stakeholders Clinical development experts Statistical… more
    AbbVie (12/06/25)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Princeton, NJ)
    …& completeness of all data types (eCRF and non eCRF) collected in BMS clinical trials from study start to database lock. **Position Summary** The Senior ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...not limited to: **Project Management and Leadership** + Provides clinical data management leadership within the study more
    Bristol Myers Squibb (01/07/26)
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  • Associate Director, Regulatory Affairs…

    Sumitomo Pharma (Trenton, NJ)
    …relationships with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, ... general product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
    Sumitomo Pharma (10/11/25)
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