• 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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  • 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 Medical Director US Medical…

    J&J Family of Companies (Horsham, PA)
    …IBD HCP and investigator interactions, support of execution, and supervision of clinical studies of all types, including: Phase IIIb/IV, registries, real ... with experience in clinical immunology/gastroenterology and/or experience with clinical studies , registries, epidemiology or health outcomes required +… more
    J&J Family of Companies (11/05/25)
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  • Associate Principal Scientist,…

    Merck (West Point, PA)
    clinical oncology trials, guiding projects from late-stage preclinical work through clinical proof-of-concept studies . + **Translational study design** : ... imaging studies in animal models and early-phase clinical trials (Phase I), ensuring robust study ...scientists, clinical and medical leads, regulatory affairs, clinical operations , and CMC teams. + **Reporting… more
    Merck (12/03/25)
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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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  • Associate Director, Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …maintain the effectiveness of the Otsuka Quality Systems that support OPDC-sponsored clinical studies as well as drive continuous improvement. **Job ... release process for OAPI GMP release of Contract Manufacturers operations supporting clinical and commercial products. +...escalation of any situations with potential negative impacts on clinical study supplies, supply chain for commercial… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Associate Medical Director, Endocrine…

    Ascendis Pharma (Princeton, NJ)
    …groups. + Work with internal stakeholders including Commercial, Legal, Regulatory, Clinical Development, Clinical Operations , Compliance, Pharmacovigilance, ... member of the Endocrine Medical Sciences team for the US business, the Associate Medical Director supports the US Medical Director for deliverables and activities… more
    Ascendis Pharma (12/07/25)
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  • Associate Director, PV Sciences

    Taiho Oncology (Princeton, NJ)
    …with team members. + Maintain training and oversight to clinical operations /pharmacovigilance vendors supporting pharmacovigilance activities, as needed. ... and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources… more
    Taiho Oncology (11/04/25)
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  • Associate Research Scientist: LBA PK & ADA…

    ThermoFisher Scientific (Lawrenceville, NJ)
    …step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel ... frameworks for clinical research through our PPD clinical research...as per departmental guidelines * Prepare or contributes to study reports following the departmental policies and procedures. *… more
    ThermoFisher Scientific (09/18/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Trenton, NJ)
    …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to ... relevant documentation. The role collaborates cross-functionally with Quality, Lab Operations , and other stakeholders to support regulatory strategy development,… more
    GRAIL (12/03/25)
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